FR2497796A1 - Chloroformiates des alkyl esters des acides c-alkyl-tartroniques et leur procede de preparation - Google Patents
Chloroformiates des alkyl esters des acides c-alkyl-tartroniques et leur procede de preparation Download PDFInfo
- Publication number
- FR2497796A1 FR2497796A1 FR8200307A FR8200307A FR2497796A1 FR 2497796 A1 FR2497796 A1 FR 2497796A1 FR 8200307 A FR8200307 A FR 8200307A FR 8200307 A FR8200307 A FR 8200307A FR 2497796 A1 FR2497796 A1 FR 2497796A1
- Authority
- FR
- France
- Prior art keywords
- alkyl
- chloroformiates
- preparation
- alkyl esters
- tartronic
- 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.)
- Granted
Links
- 239000002253 acid Substances 0.000 title abstract description 5
- 150000007513 acids Chemical class 0.000 title abstract description 5
- 238000000034 method Methods 0.000 title description 4
- 238000002360 preparation method Methods 0.000 title description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 5
- 125000005907 alkyl ester group Chemical group 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000005587 bubbling Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000007832 Na2SO4 Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000012230 colorless oil Substances 0.000 description 2
- 150000002148 esters Chemical group 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- UQRLKWGPEVNVHT-UHFFFAOYSA-N 3,5-dichloroaniline Chemical compound NC1=CC(Cl)=CC(Cl)=C1 UQRLKWGPEVNVHT-UHFFFAOYSA-N 0.000 description 1
- ITSRLVMSQHOSEC-UHFFFAOYSA-N 3-phenyl-1,3-oxazolidine Chemical compound C1OCCN1C1=CC=CC=C1 ITSRLVMSQHOSEC-UHFFFAOYSA-N 0.000 description 1
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- -1 alkyl ester chloroformates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- VGLFNWSQUOWJQL-UHFFFAOYSA-N diethyl 2-carbonochloridoyloxy-2-methylpropanedioate Chemical compound CCOC(=O)C(C)(OC(Cl)=O)C(=O)OCC VGLFNWSQUOWJQL-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 150000001475 oxazolidinediones Chemical class 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- QQKDTTWZXHEGAQ-UHFFFAOYSA-N propyl carbonochloridate Chemical compound CCCOC(Cl)=O QQKDTTWZXHEGAQ-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/04—Formic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/02—Preparation of esters of carbonic or haloformic acids from phosgene or haloformates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT19089/81A IT1135000B (it) | 1981-01-12 | 1981-01-12 | Colorformiati di esteri alchilici di acidi c-alchil-tartronici e loro processo di preparazione |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2497796A1 true FR2497796A1 (fr) | 1982-07-16 |
FR2497796B1 FR2497796B1 (en, 2012) | 1984-04-13 |
Family
ID=11154436
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR8200307A Granted FR2497796A1 (fr) | 1981-01-12 | 1982-01-11 | Chloroformiates des alkyl esters des acides c-alkyl-tartroniques et leur procede de preparation |
Country Status (10)
Country | Link |
---|---|
US (1) | US4459239A (en, 2012) |
JP (1) | JPS57136551A (en, 2012) |
BE (1) | BE891750A (en, 2012) |
CH (1) | CH649280A5 (en, 2012) |
DE (1) | DE3200534A1 (en, 2012) |
FR (1) | FR2497796A1 (en, 2012) |
GB (1) | GB2090835B (en, 2012) |
IT (1) | IT1135000B (en, 2012) |
NL (1) | NL8200044A (en, 2012) |
SU (1) | SU1169527A3 (en, 2012) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3301670A1 (de) * | 1983-01-20 | 1984-07-26 | Bayer Ag, 5090 Leverkusen | Leimungsmittel |
GB8413155D0 (en) * | 1984-05-23 | 1984-06-27 | Ici Plc | Chemical process |
EP2658818B1 (en) | 2010-12-29 | 2021-05-19 | Soiltec GmbH | Colored composite pavement structure |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3823175A (en) * | 1971-03-19 | 1974-07-09 | Dow Chemical Co | Halogenated neopentyl chloroformates |
IT1109545B (it) * | 1978-02-24 | 1985-12-16 | Montedison Spa | Derivati di n-fenil-1,3-ossazolidin-2,4-dionifungicidi e procedimento di preparazione |
-
1981
- 1981-01-12 IT IT19089/81A patent/IT1135000B/it active
-
1982
- 1982-01-07 NL NL8200044A patent/NL8200044A/nl not_active Application Discontinuation
- 1982-01-08 JP JP57001099A patent/JPS57136551A/ja active Granted
- 1982-01-08 GB GB8200586A patent/GB2090835B/en not_active Expired
- 1982-01-11 FR FR8200307A patent/FR2497796A1/fr active Granted
- 1982-01-11 BE BE0/207030A patent/BE891750A/fr not_active IP Right Cessation
- 1982-01-11 SU SU823375054A patent/SU1169527A3/ru active
- 1982-01-11 US US06/338,619 patent/US4459239A/en not_active Expired - Fee Related
- 1982-01-11 CH CH118/82A patent/CH649280A5/it not_active IP Right Cessation
- 1982-01-11 DE DE19823200534 patent/DE3200534A1/de active Granted
Non-Patent Citations (1)
Title |
---|
NEANT * |
Also Published As
Publication number | Publication date |
---|---|
DE3200534C2 (en, 2012) | 1992-05-14 |
JPH0257535B2 (en, 2012) | 1990-12-05 |
IT1135000B (it) | 1986-08-20 |
JPS57136551A (en) | 1982-08-23 |
GB2090835B (en) | 1984-12-12 |
US4459239A (en) | 1984-07-10 |
DE3200534A1 (de) | 1982-08-26 |
NL8200044A (nl) | 1982-08-02 |
GB2090835A (en) | 1982-07-21 |
IT8119089A0 (it) | 1981-01-12 |
BE891750A (fr) | 1982-07-12 |
FR2497796B1 (en, 2012) | 1984-04-13 |
CH649280A5 (it) | 1985-05-15 |
SU1169527A3 (ru) | 1985-07-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0245156B1 (fr) | Nouveau procédé de préparation de fibrates | |
FR2497796A1 (fr) | Chloroformiates des alkyl esters des acides c-alkyl-tartroniques et leur procede de preparation | |
US4673761A (en) | Process for preparing anti-inflammatory cycloalkylidenemethylphenylacetic acid derivatives | |
CH464172A (fr) | Procédé de préparation d'acides carboxyliques -substitués | |
CH615414A5 (en, 2012) | ||
EP0037327B1 (fr) | Nouveaux dérivés substitués de l'acide 3-formyl 4-méthyl pentanoique, leur préparation et leur application à la préparation d'acide 3-formyl but-3-èn-1-oique substitué | |
EP0002408A1 (fr) | Nouveaux composés phénoxy-alcanols substitués, leur procédé de préparation et leur application en thérapeutique | |
FR2661908A1 (fr) | Procede pour preparer l'acide 2,2-dimethyl-5-(2,5-dimethylphenoxy)-pentanouique et nouveaux intermediaires pour la mise en óoeuvre de ce procede. | |
JP3212104B2 (ja) | 新規なチオアセタール化合物およびその製造方法 | |
LU84142A1 (fr) | Esters 2-methoxyphenyliques d'amino-acides n-substitues,procede pour leur preparation et compositions pharmaceutiques les contenant | |
JPS6056693B2 (ja) | ハロゲン化プロピオン酸誘導体の製法 | |
EP0167464B1 (fr) | Procédé de préparation de monocarboxylates d'hydroquinone | |
FR2589151A1 (fr) | Procede de preparation d'esters du diethyleneglycol | |
US4633013A (en) | Preparation of α-haloacetoacetic esters | |
US4582913A (en) | 5-halo-4H-1,3-dioxin-4-one compounds | |
FR2487825A1 (fr) | Procede de preparation d'esters d'acides acylazo-3 propioniques | |
FR2590894A1 (fr) | Derives d'acide amino-4 butanoique, leur procede de preparation et leur utilisation | |
FR2580644A1 (fr) | Derives de l'acide ascorbique | |
Middleton et al. | New adducts of hexafluoroacetone with hydrogen cyanide | |
FR2460918A1 (fr) | Esters de l'acide 2,2-dimethyl-3-acetoxymethyl-cyclopropane-carboxylique et procede de preparation de ces composes | |
CH426781A (fr) | Procédé pour la conversion de composés 1,2,3,4-tétrahydro-anthracènes en des composés 1,2,3,4,4a,5,12,12a-octahydronaphtacènes | |
WO1986000068A1 (en) | 5-HALO-4H-1,3-DIOXIN-4-ONE COMPOUNDS, alpha-HALO-ACETOACETIC ESTERS PREPARED FROM SUCH COMPOUNDS AND PROCESS FOR THEIR PREPARATION | |
JPH0216753B2 (en, 2012) | ||
Overberger et al. | The synthesis of some optically active C‐methylated 2‐oxohexamethyleneimines | |
JPS609497B2 (ja) | 5―オキソ―2―(β―ハロエチル)ピロリジン誘導体の製造法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |