NO116080B - - Google Patents

Info

Publication number: NO116080B
Authority: NO; Norway
Prior art keywords: formaldehyde; groups; water; dithiols; temperature
Prior art date: 1966-05-09

Application number

NO168038A

Other languages

English (en)

Norwegian (no)

Inventor

B Audouze

Y Labat

Original Assignee

Aquitaine Petrole

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.)

1966-05-09

Filing date

1967-05-08

Publication date

1969-01-27

1967-05-08 Application filed by Aquitaine Petrole filed Critical Aquitaine Petrole

1969-01-27 Publication of NO116080B publication Critical patent/NO116080B/no

Links

WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 41
150000004662 dithiols Chemical class 0.000 claims description 11
238000000034 method Methods 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 7
239000003054 catalyst Substances 0.000 claims description 4
229920006295 polythiol Polymers 0.000 claims description 3
XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 3
239000000047 product Substances 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000000203 mixture Substances 0.000 description 10
235000019256 formaldehyde Nutrition 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
239000000243 solution Substances 0.000 description 6
238000002360 preparation method Methods 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
238000001816 cooling Methods 0.000 description 4
150000002009 diols Chemical class 0.000 description 4
INBDPOJZYZJUDA-UHFFFAOYSA-N methanedithiol Chemical compound SCS INBDPOJZYZJUDA-UHFFFAOYSA-N 0.000 description 4
238000003756 stirring Methods 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
239000008098 formaldehyde solution Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
239000012264 purified product Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
229920000877 Melamine resin Polymers 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241000219492 Quercus Species 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000009950 felting Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
-1 monothioether polyols Chemical class 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000012071 phase Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
210000002966 serum Anatomy 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
230000007306 turnover Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

NO168038A 1966-05-09 1967-05-08 NO116080B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR60811A FR1487364A (fr)	1966-05-09	1966-05-09	Procédé de préparation de glycols polythioéthers

Publications (1)

Publication Number	Publication Date
NO116080B true NO116080B (de)	1969-01-27

Family

ID=8608155

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO168038A NO116080B (de)	1966-05-09	1967-05-08

Country Status (13)

Country	Link
US (1)	US3519689A (de)
AT (1)	AT269822B (de)
BE (1)	BE698147A (de)
CH (1)	CH472394A (de)
DE (1)	DE1618892B1 (de)
DK (1)	DK120336B (de)
ES (1)	ES340143A1 (de)
FR (1)	FR1487364A (de)
GB (1)	GB1177827A (de)
LU (1)	LU53605A1 (de)
NL (1)	NL6706189A (de)
NO (1)	NO116080B (de)
OA (1)	OA02426A (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3962186A (en) *	1973-08-16	1976-06-08	The Dow Chemical Company	Curable composition of a polyepoxide with a methylol derivative of a polythiol
US3968167A (en) *	1975-02-07	1976-07-06	The Dow Chemical Company	Methylol derivatives of polythiols
DE3260015D1 (en) *	1981-02-05	1984-01-12	Sandoz Ag	Novel bis- and poly-disulfides having immunostimulant activity
IT1174495B (it) *	1984-02-17	1987-07-01	Nuovo Consoricio Sanitario Nat	Composti ad attivita'ipolipemizzante
US5801290A (en) *	1994-01-11	1998-09-01	Arco Chemical Technology, L.P.	Process for making poly(thioether ether)s from diallyl ether and dithiols
CN111909365B (zh) *	2019-05-09	2022-09-20	江汉大学	一种硫醚聚酯的制备方法

1966
- 1966-05-09 FR FR60811A patent/FR1487364A/fr not_active Expired
1967
- 1967-05-02 GB GB20366/67A patent/GB1177827A/en not_active Expired
- 1967-05-03 CH CH630567A patent/CH472394A/fr not_active IP Right Cessation
- 1967-05-03 NL NL6706189A patent/NL6706189A/xx unknown
- 1967-05-03 DK DK233967AA patent/DK120336B/da unknown
- 1967-05-05 ES ES340143A patent/ES340143A1/es not_active Expired
- 1967-05-05 DE DE1967S0109746 patent/DE1618892B1/de active Pending
- 1967-05-05 LU LU53605D patent/LU53605A1/xx unknown
- 1967-05-05 OA OA52924A patent/OA02426A/xx unknown
- 1967-05-05 AT AT423667A patent/AT269822B/de active
- 1967-05-08 BE BE698147D patent/BE698147A/xx unknown
- 1967-05-08 US US636652A patent/US3519689A/en not_active Expired - Lifetime
- 1967-05-08 NO NO168038A patent/NO116080B/no unknown

Also Published As

Publication number	Publication date
US3519689A (en)	1970-07-07
DK120336B (da)	1971-05-17
ES340143A1 (es)	1968-09-01
BE698147A (de)	1967-11-18
GB1177827A (en)	1970-01-14
AT269822B (de)	1969-04-10
CH472394A (fr)	1969-05-15
NL6706189A (de)	1967-11-10
LU53605A1 (de)	1968-02-12
DE1618892B1 (de)	1972-01-05
OA02426A (fr)	1970-05-05
FR1487364A (fr)	1967-07-07

Publication	Publication Date	Title
NO168038B (no)	1991-09-30	Analogifremgangsmaate for fremstilling av terapeutisk aktive 7-oksabicykloheptan-substituerte diamider og deres kongenere prostaglandinanaloger.
US2467212A (en)	1949-04-12	Liquid urea-formaldehyde compositions
SU474994A3 (ru)	1975-06-25	Способ получени сложных полиэфиров
US3519689A (en)	1970-07-07	Process for the preparation of polythioether diols
US2228159A (en)	1941-01-07	Manufacture of cation-exchanging bodies
US2372602A (en)	1945-03-27	Process for preparation of pentaerythritol
Koch et al.	1985	Condensation reactions between phenol, formaldehyde and 5-hydroxymethylfurfural, formed as intermediate in the acid catalyzed dehydration of starchy products
US2754335A (en)	1956-07-10	Triphenylols
USRE23174E (en)	1949-11-29	Liquid urea-formaldehyde
Fenton et al.	1899	LVI.—Crystalline glycollic aldehyde
US2894971A (en)	1959-07-14	Polyfluoroalkyl p-toluenesulfonates
Korshak et al.	1975	Synthesis and properties of polycondensation polymers from compounds with asymmetric functional groups
US2572256A (en)	1951-10-23	Transparent urea-aldehyde type resins and method for producing the same
JPH01318040A (ja)	1989-12-22	芳香族ポリエーテルスルホン
US2783216A (en)	1957-02-26	Resinous products from mannich bases of aromatic polyketones with hydrogen sulfide andor polythiols
US3240764A (en)	1966-03-15	Polythiosemicarbazide chelates
US2455282A (en)	1948-11-30	Processes of preparing insolubilized sulfonates and products thereof
US2612526A (en)	1952-09-30	Pentaerythritol manufacture
US2045843A (en)	1936-06-30	Manufacture of oxygenated
US2186272A (en)	1940-01-09	Process for the preparation of pentaerythritol
US2264371A (en)	1941-12-02	Process of alkylating phenols
Hayashi	1970	Reactions of 2, 2'-Dithiobis (2-methylpropionaldehyde)
US2181476A (en)	1939-11-28	Aliphatic hydroxy-ether ketones
US3121709A (en)	1964-02-18	Resinous reaction products derived from lignins
CN111072532A (zh)	2020-04-28	一种1，2，3-三巯基丙烷的制备方法