SU554809A3 - Способ получени циклопропанкарбоновых кислот - Google Patents
Способ получени циклопропанкарбоновых кислотInfo
- Publication number
- SU554809A3 SU554809A3 SU2014993A SU2014993A SU554809A3 SU 554809 A3 SU554809 A3 SU 554809A3 SU 2014993 A SU2014993 A SU 2014993A SU 2014993 A SU2014993 A SU 2014993A SU 554809 A3 SU554809 A3 SU 554809A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- solution
- general formula
- carboxylic acids
- cyclopropanecarboxylic
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 11
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 title claims description 7
- -1 polymethylene chain Polymers 0.000 claims description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 4
- YVPJCJLMRRTDMQ-UHFFFAOYSA-N ethyl diazoacetate Chemical compound CCOC(=O)C=[N+]=[N-] YVPJCJLMRRTDMQ-UHFFFAOYSA-N 0.000 claims description 3
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229910000365 copper sulfate Inorganic materials 0.000 claims description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 2
- SHQSVMDWKBRBGB-UHFFFAOYSA-N cyclobutanone Chemical compound O=C1CCC1 SHQSVMDWKBRBGB-UHFFFAOYSA-N 0.000 claims description 2
- 230000026030 halogenation Effects 0.000 claims description 2
- 238000005658 halogenation reaction Methods 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- 239000000243 solution Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 210000004885 white matter Anatomy 0.000 description 2
- CULDOFBSBZAHMP-UHFFFAOYSA-N 1,2,2,3,3-pentamethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C)(C)C1(C)C(O)=O CULDOFBSBZAHMP-UHFFFAOYSA-N 0.000 description 1
- RTGNJWAJIYCAGB-UHFFFAOYSA-N 1-bromo-3,3-dimethylspiro[3.5]nonan-2-one Chemical compound BrC1C(C(C11CCCCC1)(C)C)=O RTGNJWAJIYCAGB-UHFFFAOYSA-N 0.000 description 1
- FLWOPBVTWAAMFT-UHFFFAOYSA-N 2,2,3,3-tetramethylcyclobutan-1-one Chemical compound CC1(C)CC(=O)C1(C)C FLWOPBVTWAAMFT-UHFFFAOYSA-N 0.000 description 1
- SFHVXKNMCGSLAR-UHFFFAOYSA-N 2,2,3,3-tetramethylcyclopropanecarboxylic acid Chemical compound CC1(C)C(C(O)=O)C1(C)C SFHVXKNMCGSLAR-UHFFFAOYSA-N 0.000 description 1
- OXKYWMXNHAZFCB-UHFFFAOYSA-N 2,2,3-trimethyl-3-phenylcyclopropane-1-carboxylic acid Chemical compound CC1(C(C1(C1=CC=CC=C1)C)C(=O)O)C OXKYWMXNHAZFCB-UHFFFAOYSA-N 0.000 description 1
- PXPDZZKCEUYSHE-UHFFFAOYSA-N 2,2-dimethylspiro[2.3]hexane-1-carboxylic acid Chemical compound CC1(C)C(C(O)=O)C11CCC1 PXPDZZKCEUYSHE-UHFFFAOYSA-N 0.000 description 1
- BXYGKRALMMMKDJ-UHFFFAOYSA-N 2-bromo-2,3,3,4,4-pentamethylcyclobutan-1-one Chemical compound BrC1(C(C(C1=O)(C)C)(C)C)C BXYGKRALMMMKDJ-UHFFFAOYSA-N 0.000 description 1
- BANQGZHQUZTFRZ-UHFFFAOYSA-N 4-bromo-2,2,3-trimethyl-3-propylcyclobutan-1-one Chemical compound BrC1C(C(C1=O)(C)C)(CCC)C BANQGZHQUZTFRZ-UHFFFAOYSA-N 0.000 description 1
- GLAISTHAZUQDCE-UHFFFAOYSA-N CC1(C)C(Br)C(=O)C1(C)C Chemical compound CC1(C)C(Br)C(=O)C1(C)C GLAISTHAZUQDCE-UHFFFAOYSA-N 0.000 description 1
- QGPDMGSHNRUGMV-UHFFFAOYSA-N CC1(C)C(C(O)=O)C11CC1 Chemical compound CC1(C)C(C(O)=O)C11CC1 QGPDMGSHNRUGMV-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- KTHXBEHDVMTNOH-UHFFFAOYSA-N cyclobutanol Chemical compound OC1CCC1 KTHXBEHDVMTNOH-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- URWAJWIAIPFPJE-YFMIWBNJSA-N sisomycin Chemical compound O1C[C@@](O)(C)[C@H](NC)[C@@H](O)[C@H]1O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](CC=C(CN)O2)N)[C@@H](N)C[C@H]1N URWAJWIAIPFPJE-YFMIWBNJSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/12—Saturated polycyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O 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
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/457—Saturated compounds containing a keto group being part of a ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/457—Saturated compounds containing a keto group being part of a ring containing halogen
- C07C49/467—Saturated compounds containing a keto group being part of a ring containing halogen polycyclic
- C07C49/473—Saturated compounds containing a keto group being part of a ring containing halogen polycyclic a keto group being part of a condensed ring system
- C07C49/477—Saturated compounds containing a keto group being part of a ring containing halogen polycyclic a keto group being part of a condensed ring system having two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
- C07C49/697—Unsaturated compounds containing a keto groups being part of a ring containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1819573A GB1437832A (en) | 1973-04-16 | 1973-04-16 | Halocyclobutanones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU554809A3 true SU554809A3 (ru) | 1977-04-15 |
Family
ID=10108286
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2014993A SU554809A3 (ru) | 1973-04-16 | 1974-04-10 | Способ получени циклопропанкарбоновых кислот |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS5810371B2 (enExample) |
| BE (1) | BE813520A (enExample) |
| BR (1) | BR7402924D0 (enExample) |
| CH (1) | CH589584A5 (enExample) |
| DD (1) | DD113347A5 (enExample) |
| DE (1) | DE2417615A1 (enExample) |
| FR (1) | FR2225407B1 (enExample) |
| GB (1) | GB1437832A (enExample) |
| HU (1) | HU168443B (enExample) |
| IL (1) | IL44599A (enExample) |
| IT (1) | IT1005785B (enExample) |
| NL (1) | NL189756C (enExample) |
| SU (1) | SU554809A3 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1051454A (en) * | 1975-05-21 | 1979-03-27 | Marinus J. Van Den Brink | Process for the preparation of cyclobutanones |
| GB1571581A (en) * | 1976-01-06 | 1980-07-16 | Shell Int Research | Process for the preparation of 2-halocyclobutanones and cyclopropane carbolic acids derived therefrom |
| DE2638356A1 (de) * | 1976-08-26 | 1978-03-02 | Bayer Ag | Verfahren zur herstellung vinylsubstituierter cyclopropancarbonsaeureester |
| DE2813336A1 (de) * | 1977-03-31 | 1978-10-05 | Ciba Geigy Ag | 2-(2',2'-dihalogenvinyl)- und 2-(2', 2',2'-trihalogenaethyl)-cyclobutanone |
| DE2813337A1 (de) * | 1977-03-31 | 1978-10-05 | Ciba Geigy Ag | Verfahren zur herstellung von 2-(2', 2',2'-trihalogenaethyl)-4-halogencyclobutan1-onen |
| DE3220730A1 (de) * | 1982-06-02 | 1983-12-08 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von 2,2-dimethyl-3-aryl-cyclopropan-carbonsaeuren (carbonsaeureestern), neue zwischenprodukte hierfuer und verfahren zu deren herstellung |
| US6160134A (en) * | 1997-12-24 | 2000-12-12 | Bristol-Myers Squibb Co. | Process for preparing chiral cyclopropane carboxylic acids and acyl guanidines |
-
1973
- 1973-04-16 GB GB1819573A patent/GB1437832A/en not_active Expired
-
1974
- 1974-04-05 IT IT42674/74A patent/IT1005785B/it active
- 1974-04-10 FR FR7412630A patent/FR2225407B1/fr not_active Expired
- 1974-04-10 BE BE1005867A patent/BE813520A/xx not_active IP Right Cessation
- 1974-04-10 JP JP49040129A patent/JPS5810371B2/ja not_active Expired
- 1974-04-10 HU HUSE1720A patent/HU168443B/hu not_active IP Right Cessation
- 1974-04-10 DE DE2417615A patent/DE2417615A1/de not_active Withdrawn
- 1974-04-10 BR BR2924/74A patent/BR7402924D0/pt unknown
- 1974-04-10 IL IL44599A patent/IL44599A/en unknown
- 1974-04-10 SU SU2014993A patent/SU554809A3/ru active
- 1974-04-10 CH CH502474A patent/CH589584A5/xx not_active IP Right Cessation
- 1974-04-10 DD DD177810A patent/DD113347A5/xx unknown
- 1974-04-11 NL NLAANVRAGE7404949,A patent/NL189756C/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IL44599A0 (en) | 1974-06-30 |
| NL7404949A (enExample) | 1974-10-18 |
| DE2417615A1 (de) | 1974-11-07 |
| IT1005785B (it) | 1976-09-30 |
| GB1437832A (en) | 1976-06-03 |
| BR7402924D0 (pt) | 1974-11-19 |
| IL44599A (en) | 1977-02-28 |
| HU168443B (enExample) | 1976-04-28 |
| FR2225407B1 (enExample) | 1976-06-25 |
| BE813520A (fr) | 1974-10-10 |
| JPS5030846A (enExample) | 1975-03-27 |
| DD113347A5 (enExample) | 1975-06-05 |
| FR2225407A1 (enExample) | 1974-11-08 |
| NL189756C (nl) | 1993-07-16 |
| CH589584A5 (enExample) | 1977-07-15 |
| JPS5810371B2 (ja) | 1983-02-25 |
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