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ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyran compounds >METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE

METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE

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CAS:4160-61-6
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METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE manufacturers

METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Basic information
Product Name:METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE
Synonyms:METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE;4-OXO-TETRAHYDRO-THIOPYRAN-3-CARBOXYLIC ACID METHYL ESTER;Methyl tetrahydro-4-oxo-2H-thiopyran-3-carboxylate ,96%;Methyl 4-oxotetrahydrothiopyran-3-carboxylate;3-(Carbomethoxy)tetrahydrothiopyran-4-one;3-Carbomethoxytetrahydro-1,4-thiapyrone;3-Methoxycarbonyl-4-thianone;methyl 4-oxo-tetrahydro-2H-thiopyran-3-carboxylate
CAS:4160-61-6
MF:C7H10O3S
MW:174.22
EINECS:145-852-9
Product Categories:
Mol File:4160-61-6.mol
METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Structure
METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Chemical Properties
Boiling point 285℃
density 1.244
Fp 137℃
storage temp. Sealed in dry,Room Temperature
pka10.41±0.20(Predicted)
form Liquid or Solid
color Clear colorless to pale yellow
Safety Information
Risk Statements 36/37/38
Safety Statements 23-26-36/37/39
HS Code 29349990
MSDS Information
METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Usage And Synthesis
Chemical PropertiesLight pink liquid
Synthesis
Dimethyl 3,3'-thiodipropanoate

4131-74-2

METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE

4160-61-6

General procedure for the synthesis of methyl tetrahydro-4-oxo-2H-thiopyran-3-carboxylate from dimethyl 3,3'-thiodipropionate: 2.7098 g of NaH (60%) was added to a dry 250 ml three-necked flask, followed by the addition of 40 ml of anhydrous tetrahydrofuran (THF) and stirring for 10 min at room temperature. Dimethyl 3,3'-thiodipropionate (10.1015 g) dissolved in THF was added slowly dropwise. After dropwise addition, the reaction mixture was heated to reflux for about 1 hour. The reflux was continued for 1 hour after rinsing the dropping funnel with 10 ml of THF. The reaction was stopped and cooled to room temperature. The pH of the reaction solution was adjusted to 6-7 with 2% hydrochloric acid and then extracted with dichloromethane (30 ml x 3). The organic layers were combined, washed with saturated sodium chloride solution, collected and dried over anhydrous sodium sulfate. After filtration, the solvent was removed under reduced pressure to give 7.5639 g of a yellow oily liquid product in 88.7% yield.

References[1] Synthesis, 2007, # 10, p. 1584 - 1586
[2] Patent: CN104086562, 2016, B. Location in patent: Paragraph 0136; 0137
[3] Patent: CN105153190, 2017, B. Location in patent: Paragraph 0134; 0165; 0166
[4] Organic Letters, 2018, vol. 20, # 19, p. 6104 - 6107
[5] Journal of the American Chemical Society, 1997, vol. 119, # 18, p. 4285 - 4291
METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Preparation Products And Raw materials
Raw materialsDimethyl 3,3'-thiodipropanoate-->Methyl 3-mercaptopropionate-->acrylic acid methyl ester
Preparation Products7,8-Dihydro-5H-thiopyrano[4,3-d]pyriMidine-2,4-diol
Tag:METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE(4160-61-6) Related Product Information
2H-Thiopyran-4-carboxylic acid, tetrahydro-, Methyl ester, 1,1-dioxide 1,1-Dioxo-hexahydro-1l6-thiopyran-4-carboxylic acid DELTA-TRIDECANOLACTONE Tetrahydro-2H-pyran-4-yl methanesulfonate 2-HYDROXYTETRAHYDROPYRAN Methyl 2-oxotetrahydrofuran-3-carboxylate Tetrahydro-5-oxo-2- furancarboxyli Tetrahydro-2H-thiopyran-4-amine ethyl tetrahydro-2H-pyran-2-carboxylate METHYL TETRAHYDROPYRAN-3-CARBOXYLATE Thian-4-one S-oxide Tetrahydrothiopyran-4-one oxiMe Tetrahydro-4-oxo-3-furoic acid ethyl ester Tetrahydropyran-4-boronic acid pinacol ester METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Thiane Tetrahydrothiopyran-4-one ETHYL 4-OXO-TETRAHYDRO-3-THIOPYRANCARBOXYLATE

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