IL24343A - Halogen-containing diphenyl ethers and sulfides - Google Patents

Halogen-containing diphenyl ethers and sulfides

Info

Publication number: IL24343A
Authority: IL; Israel
Prior art keywords: ether; sulfides; parts; melting point; bromo
Prior art date: 1964-09-21

Application number

IL24343A

Other languages

English (en)

Original Assignee

Monsanto Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1964-09-21

Filing date

1965-09-20

Publication date

1970-01-29

1965-09-20 Application filed by Monsanto Co filed Critical Monsanto Co

1970-01-29 Publication of IL24343A publication Critical patent/IL24343A/en

Links

USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 title claims description 4
229910052736 halogen Inorganic materials 0.000 title claims description 4
150000002367 halogens Chemical class 0.000 title claims description 4
150000003568 thioethers Chemical class 0.000 title description 8
150000001875 compounds Chemical class 0.000 claims description 16
239000012530 fluid Substances 0.000 claims description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
229910052801 chlorine Chemical group 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
125000001246 bromo group Chemical group Br* 0.000 claims description 3
239000000460 chlorine Chemical group 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 3
229910052794 bromium Inorganic materials 0.000 claims 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
229910052760 oxygen Inorganic materials 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
238000002844 melting Methods 0.000 description 20
230000008018 melting Effects 0.000 description 20
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
239000000203 mixture Substances 0.000 description 6
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
238000009835 boiling Methods 0.000 description 5
125000001309 chloro group Chemical group Cl* 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
239000003518 caustics Substances 0.000 description 3
239000002826 coolant Substances 0.000 description 3
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
JSRLURSZEMLAFO-UHFFFAOYSA-N 1,3-dibromobenzene Chemical compound BrC1=CC=CC(Br)=C1 JSRLURSZEMLAFO-UHFFFAOYSA-N 0.000 description 2
SWJPEBQEEAHIGZ-UHFFFAOYSA-N 1,4-dibromobenzene Chemical compound BrC1=CC=C(Br)C=C1 SWJPEBQEEAHIGZ-UHFFFAOYSA-N 0.000 description 2
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 2
HORNXRXVQWOLPJ-UHFFFAOYSA-N 3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1 HORNXRXVQWOLPJ-UHFFFAOYSA-N 0.000 description 2
229910021591 Copper(I) chloride Inorganic materials 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
239000002585 base Substances 0.000 description 2
125000006267 biphenyl group Chemical group 0.000 description 2
235000017168 chlorine Nutrition 0.000 description 2
OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 2
229940045803 cuprous chloride Drugs 0.000 description 2
238000004821 distillation Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 2
229940031826 phenolate Drugs 0.000 description 2
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
238000010992 reflux Methods 0.000 description 2
HPRGYUWRGCTBAV-UHFFFAOYSA-N 1-chloro-3-(4-chlorophenoxy)benzene Chemical compound C1=CC(Cl)=CC=C1OC1=CC=CC(Cl)=C1 HPRGYUWRGCTBAV-UHFFFAOYSA-N 0.000 description 1
URUJZHZLCCIILC-UHFFFAOYSA-N 1-chloro-4-(4-chlorophenoxy)benzene Chemical compound C1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1 URUJZHZLCCIILC-UHFFFAOYSA-N 0.000 description 1
VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
SYKNUAWMBRIEKB-UHFFFAOYSA-N [Cl].[Br] Chemical compound [Cl].[Br] SYKNUAWMBRIEKB-UHFFFAOYSA-N 0.000 description 1
238000013019 agitation Methods 0.000 description 1
238000004378 air conditioning Methods 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000013016 damping Methods 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical class C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
230000009970 fire resistant effect Effects 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
KSLKDKJNBJAMEG-UHFFFAOYSA-M potassium;2-chlorophenolate Chemical compound [K+].[O-]C1=CC=CC=C1Cl KSLKDKJNBJAMEG-UHFFFAOYSA-M 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000003464 sulfur compounds Chemical class 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/042—Alcohols; Ethers; Aldehydes; Ketones
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/086—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing sulfur atoms bound to carbon atoms of six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/32—Light or X-ray resistance
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyrrole Compounds (AREA)
Indole Compounds (AREA)

IL24343A 1964-09-21 1965-09-20 Halogen-containing diphenyl ethers and sulfides IL24343A (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US39804864A	1964-09-21	1964-09-21
US398093A US3371120A (en)	1964-09-21	1964-09-21	3, 4'-halogen-containing diphenyl ethers and thio ethers
US68303467A	1967-04-03	1967-04-03

Publications (1)

Publication Number	Publication Date
IL24343A true IL24343A (en)	1970-01-29

Family

ID=27410287

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL24343A IL24343A (en)	1964-09-21	1965-09-20	Halogen-containing diphenyl ethers and sulfides

Country Status (9)

Country	Link
US (2)	US3371120A (de)
BE (1)	BE669888A (de)
CH (1)	CH485839A (de)
DE (1)	DE1594506A1 (de)
GB (1)	GB1121484A (de)
IL (1)	IL24343A (de)
LU (1)	LU49503A1 (de)
NL (1)	NL6512286A (de)
SE (1)	SE320674B (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3481986A (en) *	1966-10-21	1969-12-02	Marathon Oil Co	Chemical process for the production of carbonyl addition compounds
US4502973A (en) *	1981-06-19	1985-03-05	National Research Development Corporation	Electroviscous fluids
US4483788A (en) *	1982-03-25	1984-11-20	The National Research Development Corp.	Electric field responsive fluids
DE3508212A1 (de) *	1983-09-08	1986-09-11	Chemische Fabrik Kalk GmbH, 5000 Köln	Schwer entflammbare hydraulikfluessigkeit
DE3402863A1 (de) *	1984-01-27	1985-08-01	Hydrocor-Forschungs- und Analytik GmbH, 1000 Berlin	Bromhaltige benzyltoluol-derivate, verfahren zu ihrer herstellung und deren verwendung
US4766253A (en) *	1987-05-04	1988-08-23	Ciba-Geigy Corporation	Process for preparing chlorinated diphenyl ethers
US5068459A (en) *	1989-04-19	1991-11-26	Mitsui Toatsu Chemicals, Inc.	Process for producing m-phenoxybenzyl alcohol
US5405543A (en) *	1989-07-04	1995-04-11	Kabushiki Kaisha Tokai Rika Denki Seisakusho	Grease for copper contact
CN103073408A (zh) *	2013-01-06	2013-05-01	扬州市天平化工厂有限公司	二氯二苯醚酮的制备方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3072728A (en) *	1960-03-24	1963-01-08	Monsanto Chemicals	Method of preparing halogenated diphenyl compounds

1964
- 1964-09-21 US US398093A patent/US3371120A/en not_active Expired - Lifetime
1965
- 1965-09-20 DE DE19651594506 patent/DE1594506A1/de active Pending
- 1965-09-20 IL IL24343A patent/IL24343A/en unknown
- 1965-09-21 GB GB40179/65A patent/GB1121484A/en not_active Expired
- 1965-09-21 LU LU49503A patent/LU49503A1/xx unknown
- 1965-09-21 BE BE669888D patent/BE669888A/xx unknown
- 1965-09-21 CH CH1300165A patent/CH485839A/de not_active IP Right Cessation
- 1965-09-21 NL NL6512286A patent/NL6512286A/xx unknown
- 1965-09-21 SE SE12252/65A patent/SE320674B/xx unknown
1967
- 1967-04-03 US US683034A patent/US3472782A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
SE320674B (de)	1970-02-16
GB1121484A (en)	1968-07-31
LU49503A1 (de)	1966-03-21
DE1594506A1 (de)	1972-02-17
CH485839A (de)	1970-02-15
US3371120A (en)	1968-02-27
US3472782A (en)	1969-10-14
NL6512286A (de)	1966-03-22
BE669888A (de)	1966-03-21

Publication	Publication Date	Title
IL24343A (en)	1970-01-29	Halogen-containing diphenyl ethers and sulfides
US2671799A (en)	1954-03-09	Perhalocarbon compounds and method of preparing them
US3321529A (en)	1967-05-23	Polyphenyl thioethers
US3538166A (en)	1970-11-03	Halogenated polyphenyl thioethers and method for preparation
US3450770A (en)	1969-06-17	Polyphenyl thioethers
US2273471A (en)	1942-02-17	Di (arylalkyl) sulphide
US2438599A (en)	1948-03-30	Lubricating oil composition
US2185008A (en)	1939-12-26	Di-alkylbenzenoid sulphides and process for their production
US3634519A (en)	1972-01-11	Process for the production of diarylethers
US2483499A (en)	1949-10-04	Lube oil additives and preparation thereof
US2998454A (en)	1961-08-29	Substituted phenyl biphenylyl sulfones and their preparation
US2998453A (en)	1961-08-29	Phenoxy diphenyl sulfones and their preparation
US2278719A (en)	1942-04-07	Method of synthesizing sulphurbearing, high molecular weight hydrocarbons
US3397244A (en)	1968-08-13	Process for production of diaryl and di (alkaryl) sulfides
US2221808A (en)	1940-11-19	Halo-substituted polyalkyl phenols
US3491024A (en)	1970-01-20	2,6-disubstituted primary aryl phosphites,their salts and phosphorodihalidites and processes for the manufacture thereof
US2515129A (en)	1950-07-11	Lubricant composition
US3957666A (en)	1976-05-18	Phenoxybiphenyl and phenoxyterphenyl compounds and compositions
US3221058A (en)	1965-11-30	Aromatic polyethers
US3247245A (en)	1966-04-19	Alkylated polyphenyl ether sulfonates
US3441615A (en)	1969-04-29	Alkoxy aromatic ethers
US2185009A (en)	1939-12-26	Di-alkylhalobenzenoid sulphides and the process for producing the same
US2107905A (en)	1938-02-08	Chlorinated aralkyl ketones
US3053901A (en)	1962-09-11	Polyaryl sulphide
US2467028A (en)	1949-04-12	Nitro alkane sulfonyl chlorides