JPS6223739B2 - - Google Patents
Info
- Publication number
- JPS6223739B2 JPS6223739B2 JP53139481A JP13948178A JPS6223739B2 JP S6223739 B2 JPS6223739 B2 JP S6223739B2 JP 53139481 A JP53139481 A JP 53139481A JP 13948178 A JP13948178 A JP 13948178A JP S6223739 B2 JPS6223739 B2 JP S6223739B2
- Authority
- JP
- Japan
- Prior art keywords
- thionyl chloride
- butyrolactone
- hours
- alcohol
- producing
- 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
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 28
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical class O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 11
- 229930188620 butyrolactone Natural products 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 150000002596 lactones Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- -1 chlorocarboxylic acid ester Chemical class 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 2
- QGLBZNZGBLRJGS-UHFFFAOYSA-N Dihydro-3-methyl-2(3H)-furanone Chemical compound CC1CCOC1=O QGLBZNZGBLRJGS-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- ALZLTHLQMAFAPA-UHFFFAOYSA-N 3-Methylbutyrolactone Chemical compound CC1COC(=O)C1 ALZLTHLQMAFAPA-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- KFZMSGVFBACQDK-UHFFFAOYSA-N ethyl 3-chloropentanoate Chemical compound CCOC(=O)CC(Cl)CC KFZMSGVFBACQDK-UHFFFAOYSA-N 0.000 description 1
- HSMWWODOXVRNOR-UHFFFAOYSA-N ethyl 4-chloro-2-methylbutanoate Chemical compound CCOC(=O)C(C)CCCl HSMWWODOXVRNOR-UHFFFAOYSA-N 0.000 description 1
- OJAYUEGXOWQYTB-UHFFFAOYSA-N ethyl 4-chloropentanoate Chemical compound CCOC(=O)CCC(C)Cl OJAYUEGXOWQYTB-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229940040102 levulinic acid Drugs 0.000 description 1
- BHQQXAOBIZQEGI-UHFFFAOYSA-N methyl 2-chlorobutanoate Chemical compound CCC(Cl)C(=O)OC BHQQXAOBIZQEGI-UHFFFAOYSA-N 0.000 description 1
- YCQMBQQPRXPRAA-UHFFFAOYSA-N methyl 4-chloro-3-methylbutanoate Chemical compound COC(=O)CC(C)CCl YCQMBQQPRXPRAA-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/307—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/363—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- 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
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
-
- 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
- C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
- C07C53/19—Acids containing three or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/63—Halogen-containing esters of saturated acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2751134A DE2751134C2 (de) | 1977-11-16 | 1977-11-16 | Verfahren zur Herstellung von γ-Chlorcarbonsäureestern |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5479224A JPS5479224A (en) | 1979-06-25 |
| JPS6223739B2 true JPS6223739B2 (it) | 1987-05-25 |
Family
ID=6023827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13948178A Granted JPS5479224A (en) | 1977-11-16 | 1978-11-14 | Manufacture of gammaachlorcarboxylic acid ester |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS5479224A (it) |
| BE (1) | BE872028A (it) |
| CA (1) | CA1136643A (it) |
| CH (1) | CH636593A5 (it) |
| DE (1) | DE2751134C2 (it) |
| FR (1) | FR2409254A1 (it) |
| GB (1) | GB2008111B (it) |
| IL (1) | IL55933A (it) |
| IT (1) | IT1157707B (it) |
| NL (1) | NL7808304A (it) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI86889C (fi) * | 1984-03-29 | 1992-10-26 | Lonza Ag | Foerfarande foer framstaellning av av l-karnitin pao mikrobiologiskt saett |
| DE3538133A1 (de) * | 1985-10-26 | 1987-04-30 | Huels Chemische Werke Ag | Verfahren zur herstellung von reinen, chlorfreien cyclopropancarbonsaeureestern |
| JPH0291049A (ja) * | 1988-09-21 | 1990-03-30 | Lonza Ag | ｒ―ブチロベタインの製造方法 |
| DE4412316A1 (de) * | 1994-04-11 | 1995-10-12 | Basf Ag | Verfahren zur Herstellung von o-Chlormethylbenzoesäurechloriden |
| US6552217B2 (en) | 2000-08-01 | 2003-04-22 | Eastman Chemical Company | Process for the preparation of alkyl 1-methylcyclopropanecarboxylate |
| CN106631777B (zh) * | 2016-11-30 | 2019-02-19 | 浙江大学 | 合成γ-氯丁酸甲酯的方法 |
| CN117510328B (zh) * | 2023-12-29 | 2024-04-12 | 山东京新药业有限公司 | 一种4-氯丁酸甲酯的制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3927074A (en) * | 1974-06-19 | 1975-12-16 | Olin Corp | Preparation of halobutyrate esters |
-
1977
- 1977-11-16 DE DE2751134A patent/DE2751134C2/de not_active Expired
-
1978
- 1978-08-08 NL NL7808304A patent/NL7808304A/xx not_active Application Discontinuation
- 1978-10-27 CA CA000314569A patent/CA1136643A/en not_active Expired
- 1978-11-08 GB GB7843737A patent/GB2008111B/en not_active Expired
- 1978-11-10 FR FR7831873A patent/FR2409254A1/fr active Granted
- 1978-11-14 BE BE6046668A patent/BE872028A/xx not_active IP Right Cessation
- 1978-11-14 JP JP13948178A patent/JPS5479224A/ja active Granted
- 1978-11-14 IL IL55933A patent/IL55933A/xx unknown
- 1978-11-15 IT IT51914/78A patent/IT1157707B/it active
- 1978-11-15 CH CH1175178A patent/CH636593A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CH636593A5 (de) | 1983-06-15 |
| IT1157707B (it) | 1987-02-18 |
| IT7851914A0 (it) | 1978-11-15 |
| GB2008111A (en) | 1979-05-31 |
| FR2409254A1 (fr) | 1979-06-15 |
| NL7808304A (nl) | 1979-05-18 |
| CA1136643A (en) | 1982-11-30 |
| IL55933A (en) | 1982-02-28 |
| IL55933A0 (en) | 1979-01-31 |
| GB2008111B (en) | 1982-04-15 |
| DE2751134A1 (de) | 1979-05-17 |
| JPS5479224A (en) | 1979-06-25 |
| BE872028A (fr) | 1979-05-14 |
| FR2409254B1 (it) | 1984-10-05 |
| DE2751134C2 (de) | 1986-04-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA010883B1 (ru) | Способ получения гексагидрофуро[2,3-в]фуран-3-ола | |
| US4127604A (en) | Process for the preparation of acetic acid derivatives | |
| JPS6223739B2 (it) | ||
| JP2013227345A (ja) | ハーフエステルの合成方法 | |
| WO1988005773A1 (en) | Process for preparing tetrakis (3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionyloxymethyl)methane | |
| JPH0129783B2 (it) | ||
| JPH10279527A (ja) | ２−ヘキシルデカニル（メタ）アクリレートおよびその製造方法 | |
| JP3357076B2 (ja) | ジカルボン酸モノエステルの製造方法 | |
| JPH0696564B2 (ja) | α−（ω−ヒドロキシアルキル）フルフリルアルコ−ル及びその製造法 | |
| JP3254746B2 (ja) | 末端アセチレン化合物およびその製造法 | |
| JPH11322643A (ja) | クロロアルキン類およびアルキニルアミン類の製造方法 | |
| US4021425A (en) | Process for producing enone intermediates | |
| JP3159413B2 (ja) | ３−置換−４−ヒドロキシ−２−ブテノライドの製造方法 | |
| JP2617017B2 (ja) | ソルビン酸の還元方法 | |
| JPH0480910B2 (it) | ||
| WO2024110278A1 (en) | Production of panthenol | |
| KR940000197B1 (ko) | 이소프로필 3s-아미노-2r-히드록시-알카노에이트의 제조 방법 및 그의 중간체 | |
| JP2005139068A (ja) | α―アセチル−γ―ブチロラクトン誘導体の製造方法 | |
| JPWO2013038931A1 (ja) | ２−オキソ−２Ｈ−シクロヘプタ［ｂ］フラン類縁体の製造方法 | |
| EP0641335A1 (en) | Free radical-catalyzed synthesis of benzoprostacyclins | |
| SU589905A3 (ru) | Способ получени йодалкенильных соединений | |
| JP2852126B2 (ja) | ２−フルオロイソ酪酸またはそのエステルの製造方法 | |
| US3819704A (en) | Conversion of saturated carboxylic acids to n-alkylated aldimines | |
| JP3041999B2 (ja) | 光学活性グリセロールエステルの製造方法 | |
| KR800001178B1 (ko) | 아세토 나이트릴유도체의 제조방법 |