GB1374323A - Production of monohaloacyl halides - Google Patents
Production of monohaloacyl halidesInfo
- Publication number
- GB1374323A GB1374323A GB4505372A GB4505372A GB1374323A GB 1374323 A GB1374323 A GB 1374323A GB 4505372 A GB4505372 A GB 4505372A GB 4505372 A GB4505372 A GB 4505372A GB 1374323 A GB1374323 A GB 1374323A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbonate
- glycol
- ketene
- methyl
- halides
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 150000004820 halides Chemical class 0.000 title abstract 5
- 239000002904 solvent Substances 0.000 abstract 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 abstract 3
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract 2
- -1 alkoxyalkyl ester Chemical class 0.000 abstract 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000005676 cyclic carbonates Chemical class 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- UKDOTCFNLHHKOF-FGRDZWBJSA-N (z)-1-chloroprop-1-ene;(z)-1,2-dichloroethene Chemical group C\C=C/Cl.Cl\C=C/Cl UKDOTCFNLHHKOF-FGRDZWBJSA-N 0.000 abstract 1
- 229940058015 1,3-butylene glycol Drugs 0.000 abstract 1
- BTVWZWFKMIUSGS-UHFFFAOYSA-N 2-methylpropane-1,2-diol Chemical compound CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 abstract 1
- RZGZTQYTDRQOEY-UHFFFAOYSA-N 2-phenylethenone Chemical compound O=C=CC1=CC=CC=C1 RZGZTQYTDRQOEY-UHFFFAOYSA-N 0.000 abstract 1
- TXQPIYKVIOKFAB-UHFFFAOYSA-N 4,4,5,5-tetrachloro-1,3-dioxolan-2-one Chemical compound ClC1(Cl)OC(=O)OC1(Cl)Cl TXQPIYKVIOKFAB-UHFFFAOYSA-N 0.000 abstract 1
- UAUBPLHWJOYCHE-UHFFFAOYSA-N 4,5-diethyl-1,3-dioxolan-2-one Chemical compound CCC1OC(=O)OC1CC UAUBPLHWJOYCHE-UHFFFAOYSA-N 0.000 abstract 1
- LWLOKSXSAUHTJO-UHFFFAOYSA-N 4,5-dimethyl-1,3-dioxolan-2-one Chemical compound CC1OC(=O)OC1C LWLOKSXSAUHTJO-UHFFFAOYSA-N 0.000 abstract 1
- LFEAJBLOEPTINE-UHFFFAOYSA-N 4-(chloromethyl)-1,3-dioxolan-2-one Chemical compound ClCC1COC(=O)O1 LFEAJBLOEPTINE-UHFFFAOYSA-N 0.000 abstract 1
- OVDQEUFSGODEBT-UHFFFAOYSA-N 4-methyl-1,3-dioxan-2-one Chemical class CC1CCOC(=O)O1 OVDQEUFSGODEBT-UHFFFAOYSA-N 0.000 abstract 1
- ZKOGUIGAVNCCKH-UHFFFAOYSA-N 4-phenyl-1,3-dioxolan-2-one Chemical compound O1C(=O)OCC1C1=CC=CC=C1 ZKOGUIGAVNCCKH-UHFFFAOYSA-N 0.000 abstract 1
- JRFXQKZEGILCCO-UHFFFAOYSA-N 5,5-dimethyl-1,3-dioxan-2-one Chemical compound CC1(C)COC(=O)OC1 JRFXQKZEGILCCO-UHFFFAOYSA-N 0.000 abstract 1
- VNRBVNKVERHPBJ-UHFFFAOYSA-N C1(OC(C(CO1)CC)CC)=O Chemical compound C1(OC(C(CO1)CC)CC)=O VNRBVNKVERHPBJ-UHFFFAOYSA-N 0.000 abstract 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- 150000001266 acyl halides Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 abstract 1
- 235000019437 butane-1,3-diol Nutrition 0.000 abstract 1
- 150000004648 butanoic acid derivatives Chemical class 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 230000002140 halogenating effect Effects 0.000 abstract 1
- 230000026030 halogenation Effects 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical class CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 150000002561 ketenes Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 abstract 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical class CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- UYLUJGRCKKSWHS-UHFFFAOYSA-N prop-1-en-1-one Chemical compound CC=C=O UYLUJGRCKKSWHS-UHFFFAOYSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical class O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 abstract 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-M valerate Chemical class CCCCC([O-])=O NQPDZGIKBAWPEJ-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- 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
- C07C53/46—Acyl halides containing halogen outside the carbonyl halide group
- C07C53/50—Acyl halides containing halogen outside the carbonyl halide group of acids containing three or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
-
- 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
- C07C53/40—Acetyl halides
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18540271A | 1971-09-30 | 1971-09-30 | |
| US18545071A | 1971-09-30 | 1971-09-30 | |
| US18539671A | 1971-09-30 | 1971-09-30 | |
| US19264771A | 1971-10-26 | 1971-10-26 | |
| US27628272A | 1972-07-31 | 1972-07-31 | |
| US27628172A | 1972-07-31 | 1972-07-31 | |
| US00276280A US3812183A (en) | 1971-09-30 | 1972-07-31 | Preparation of monohaloacetyl halides |
| US27796172A | 1972-08-04 | 1972-08-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1374323A true GB1374323A (en) | 1974-11-20 |
Family
ID=27575105
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4505372A Expired GB1374323A (en) | 1971-09-30 | 1972-09-29 | Production of monohaloacyl halides |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS4840712A (enrdf_load_stackoverflow) |
| BE (1) | BE789467A (enrdf_load_stackoverflow) |
| CA (1) | CA985705A (enrdf_load_stackoverflow) |
| CH (1) | CH576412A5 (enrdf_load_stackoverflow) |
| DK (1) | DK153137C (enrdf_load_stackoverflow) |
| EG (1) | EG11089A (enrdf_load_stackoverflow) |
| GB (1) | GB1374323A (enrdf_load_stackoverflow) |
| IL (1) | IL40466A (enrdf_load_stackoverflow) |
| IT (1) | IT968446B (enrdf_load_stackoverflow) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RO73277A (ro) * | 1973-07-16 | 1983-08-03 | Monsanto Co,Us | Procedeu pentru prepararea halogenurilor monohaloacil |
| JPS5831768Y2 (ja) * | 1977-09-06 | 1983-07-14 | ゼネラルパッカ−株式会社 | 包装装置の非開口若しくは非充填包装袋自動回収装置 |
| JPS5442280A (en) * | 1977-09-09 | 1979-04-04 | Tenchi Kikai Kk | Device for separating each predetermined quantity of linked wrapped articles in seal wrapping machine |
| JPS5460086A (en) * | 1977-10-20 | 1979-05-15 | Kunio Tousaka | Method of preventing erroneous cutting of small bag continuous band |
| WO1998050339A1 (fr) * | 1997-05-07 | 1998-11-12 | Idemitsu Petrochemical Co., Ltd. | 1-ACETOXY-3-n-PROPOXYPROPANE ET SOLVANTS D'ETHER ALCOOL |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2862964A (en) * | 1955-07-12 | 1958-12-02 | Distillers Co Yeast Ltd | Process for producing monochloro acetyl chloride |
-
0
- BE BE789467D patent/BE789467A/xx not_active IP Right Cessation
-
1972
- 1972-09-28 EG EG397/72A patent/EG11089A/xx active
- 1972-09-29 GB GB4505372A patent/GB1374323A/en not_active Expired
- 1972-09-29 IL IL40466A patent/IL40466A/en unknown
- 1972-09-29 IT IT29877/72A patent/IT968446B/it active
- 1972-09-29 CH CH1431072A patent/CH576412A5/xx not_active IP Right Cessation
- 1972-09-29 DK DK483172A patent/DK153137C/da not_active IP Right Cessation
- 1972-09-29 JP JP47097269A patent/JPS4840712A/ja active Pending
- 1972-09-29 CA CA152,965A patent/CA985705A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE789467A (fr) | 1973-03-29 |
| IL40466A (en) | 1976-04-30 |
| IL40466A0 (en) | 1972-11-28 |
| IT968446B (it) | 1974-03-20 |
| JPS4840712A (enrdf_load_stackoverflow) | 1973-06-15 |
| DK153137B (da) | 1988-06-20 |
| CA985705A (en) | 1976-03-16 |
| CH576412A5 (enrdf_load_stackoverflow) | 1976-06-15 |
| EG11089A (en) | 1976-12-31 |
| DK153137C (da) | 1988-12-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |