SE439301B - Forfarande for kontinuerlig bildning av en syraflourid av kolmonoxid, vattenfri vetefluorid och ett olefin - Google Patents

Forfarande for kontinuerlig bildning av en syraflourid av kolmonoxid, vattenfri vetefluorid och ett olefin

Info

Publication number: SE439301B
Authority: SE; Sweden
Prior art keywords: high turbulence; olefin; reaction; reactor; reactant mixture
Prior art date: 1981-01-26

Application number

SE8200471A

Other languages

English (en)

Swedish (sv)

Other versions

SE8200471L (sv

Inventor

Jr J E Corn

Original Assignee

Ashland Oil Inc

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.)

1981-01-26

Filing date

1982-01-28

Publication date

1985-06-10

1982-01-28 Application filed by Ashland Oil Inc filed Critical Ashland Oil Inc

1983-07-29 Publication of SE8200471L publication Critical patent/SE8200471L/xx

1985-06-10 Publication of SE439301B publication Critical patent/SE439301B/sv

Links

229910002091 carbon monoxide Inorganic materials 0.000 title claims description 19
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 title claims description 13
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims description 12
238000000034 method Methods 0.000 title claims description 10
241000209140 Triticum Species 0.000 title 1
235000021307 Triticum Nutrition 0.000 title 1
150000001336 alkenes Chemical class 0.000 claims description 39
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 37
238000006243 chemical reaction Methods 0.000 claims description 34
239000000376 reactant Substances 0.000 claims description 19
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 15
229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 14
230000015572 biosynthetic process Effects 0.000 claims description 5
230000035484 reaction time Effects 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000003153 chemical reaction reagent Substances 0.000 description 12
239000007791 liquid phase Substances 0.000 description 9
239000012071 phase Substances 0.000 description 7
238000001816 cooling Methods 0.000 description 5
239000007788 liquid Substances 0.000 description 5
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
239000007789 gas Substances 0.000 description 4
-1 ethylene, propylene, butene Chemical class 0.000 description 3
230000000135 prohibitive effect Effects 0.000 description 3
239000000243 solution Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
238000006471 dimerization reaction Methods 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
150000002222 fluorine compounds Chemical class 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000012544 monitoring process Methods 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
KZDCMKVLEYCGQX-UDPGNSCCSA-N 2-(diethylamino)ethyl 4-aminobenzoate;(2s,5r,6r)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;hydrate Chemical compound O.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1.N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 KZDCMKVLEYCGQX-UDPGNSCCSA-N 0.000 description 1
FSQOYWQCIXSBNP-UHFFFAOYSA-N 2-methylpropanoyl fluoride Chemical compound CC(C)C(F)=O FSQOYWQCIXSBNP-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
238000013019 agitation Methods 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
230000000447 dimerizing effect Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
239000000463 material Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
239000000047 product Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/38—Acyl halides
- C07C53/42—Acyl halides of acids containing three or more carbon atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

SE8200471A 1981-01-26 1982-01-28 Forfarande for kontinuerlig bildning av en syraflourid av kolmonoxid, vattenfri vetefluorid och ett olefin SE439301B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/228,305 US4495110A (en)	1981-01-26	1981-01-26	Method of continuously forming an acid fluoride from carbon monoxide, anhydrous hydrogen fluoride and an olefin

Publications (2)

Publication Number	Publication Date
SE8200471L SE8200471L (sv)	1983-07-29
SE439301B true SE439301B (sv)	1985-06-10

Family

ID=22856621

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8200471A SE439301B (sv)	1981-01-26	1982-01-28	Forfarande for kontinuerlig bildning av en syraflourid av kolmonoxid, vattenfri vetefluorid och ett olefin

Country Status (19)

Country	Link
US (1)	US4495110A (it)
JP (1)	JPS6024087B2 (it)
KR (1)	KR850001371B1 (it)
AT (1)	AT386598B (it)
AU (1)	AU527823B2 (it)
BR (1)	BR8200427A (it)
CA (1)	CA1172657A (it)
CH (1)	CH649278A5 (it)
DD (1)	DD208346A5 (it)
DE (1)	DE3202292C2 (it)
ES (1)	ES8302601A1 (it)
FR (1)	FR2498593B1 (it)
GB (1)	GB2092142B (it)
IT (1)	IT1150154B (it)
MX (1)	MX157368A (it)
NL (1)	NL187806C (it)
PL (1)	PL139817B1 (it)
SE (1)	SE439301B (it)
ZA (1)	ZA82501B (it)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3213395A1 (de) *	1982-04-10	1983-10-13	Röhm GmbH, 6100 Darmstadt	Verfahren zur herstellung von isobuttersaeurefluorid bzw. isobuttersaeure
US4499029A (en) *	1983-06-15	1985-02-12	Ashland Oil, Inc.	Isobutyryl fluoride manufacture
CA1253880A (en) *	1984-06-18	1989-05-09	Carlo Scaccia	Gas-liquid process for preparing isobutyryl fluoride and reactor therefor
ES2025186B3 (es) *	1986-11-20	1992-03-16	Atochem	Procedimiento catalitico de carbonilacion de alcanos.

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3059005A (en) *		1962-10-16		Process for the production of
US2831877A (en) *	1952-03-24	1958-04-22	Studiengesellschaft Kohel Mit	Production of carboxylic acids from olefins
US2876241A (en) *	1954-05-15	1959-03-03	Studiengesellschaft Kohle Mit	Process for the production of carboxylic acids
US3005846A (en) *	1959-04-06	1961-10-24	Sinclair Refining Co	Production of acids and esters
US3065242A (en) *	1960-02-23	1962-11-20	Du Pont	Production of acyl halides, carboxylic acids and lactones
DE1226557B (de) *	1962-03-03	1966-10-13	Schering Ag	Verfahren zur Herstellung von Methyl-, AEthyl- oder Propylestern gesaettigter alpha-alkylverzweigter Fettsaeuren mit mindestens 4 Kohlenstoffatomen
FR1377834A (fr) *	1963-12-19	1964-11-06	Exxon Research Engineering Co	Procédé perfectionné de synthèse d'acides carboxyliques
NL6910591A (it) *	1969-07-10	1971-01-12
US3661951A (en) *	1969-12-01	1972-05-09	Armour Ind Chem Co	Carboxylation of olefins

1981
- 1981-01-26 US US06/228,305 patent/US4495110A/en not_active Expired - Lifetime
1982
- 1982-01-22 CA CA000395816A patent/CA1172657A/en not_active Expired
- 1982-01-26 MX MX191145A patent/MX157368A/es unknown
- 1982-01-26 AT AT0027582A patent/AT386598B/de not_active IP Right Cessation
- 1982-01-26 GB GB8202156A patent/GB2092142B/en not_active Expired
- 1982-01-26 KR KR8200312A patent/KR850001371B1/ko not_active Expired
- 1982-01-26 DD DD82236979A patent/DD208346A5/de not_active IP Right Cessation
- 1982-01-26 FR FR8201196A patent/FR2498593B1/fr not_active Expired
- 1982-01-26 IT IT19317/82A patent/IT1150154B/it active
- 1982-01-26 CH CH730/82A patent/CH649278A5/de not_active IP Right Cessation
- 1982-01-26 DE DE3202292A patent/DE3202292C2/de not_active Expired
- 1982-01-26 ES ES509885A patent/ES8302601A1/es not_active Expired
- 1982-01-26 NL NLAANVRAGE8200276,A patent/NL187806C/xx not_active IP Right Cessation
- 1982-01-26 ZA ZA82501A patent/ZA82501B/xx unknown
- 1982-01-26 BR BR8200427A patent/BR8200427A/pt unknown
- 1982-01-26 JP JP57011458A patent/JPS6024087B2/ja not_active Expired
- 1982-01-27 AU AU79893/82A patent/AU527823B2/en not_active Ceased
- 1982-01-28 SE SE8200471A patent/SE439301B/sv not_active IP Right Cessation
- 1982-02-23 PL PL1982235185A patent/PL139817B1/pl unknown

Also Published As

Publication number	Publication date
DE3202292A1 (de)	1982-08-12
JPS6024087B2 (ja)	1985-06-11
ATA27582A (de)	1988-02-15
US4495110A (en)	1985-01-22
NL8200276A (nl)	1982-08-16
BR8200427A (pt)	1982-11-30
ZA82501B (en)	1982-12-29
FR2498593A1 (fr)	1982-07-30
GB2092142A (en)	1982-08-11
PL139817B1 (en)	1987-02-28
NL187806B (nl)	1991-08-16
ES509885A0 (es)	1983-01-16
DE3202292C2 (de)	1985-06-20
IT8219317A0 (it)	1982-01-26
AU527823B2 (en)	1983-03-24
MX157368A (es)	1988-11-18
DD208346A5 (de)	1984-05-02
FR2498593B1 (fr)	1985-06-28
SE8200471L (sv)	1983-07-29
CH649278A5 (de)	1985-05-15
AT386598B (de)	1988-09-12
JPS57142939A (en)	1982-09-03
KR850001371B1 (ko)	1985-09-24
CA1172657A (en)	1984-08-14
PL235185A1 (en)	1983-03-28
GB2092142B (en)	1984-12-05
NL187806C (nl)	1992-01-16
ES8302601A1 (es)	1983-01-16
AU7989382A (en)	1982-08-05
KR830008970A (ko)	1983-12-16
IT1150154B (it)	1986-12-10

Legal Events

Date

Code

Title

Description

1995-01-31

NUG

Patent has lapsed

Ref document number: 8200471-4

Effective date: 19940810

Format of ref document f/p: F

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