Basic information Uses Safety Supplier Related
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

Basic information Uses Safety Supplier Related

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
Mol File:
4160-61-6.mol
More
Less

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

Boiling point:
285℃
Density 
1.244
Flash point:
137℃
storage temp. 
Sealed in dry,Room Temperature
pka
10.41±0.20(Predicted)
form 
Liquid or Solid
color 
Clear colorless to pale yellow
More
Less

Safety Information

Risk Statements 
36/37/38
Safety Statements 
23-26-36/37/39
HS Code 
29349990
More
Less

METHYL TETRAHYDRO-4-OXO-2H-THIOPYRAN-3-CARBOXYLATE Usage And Synthesis

Uses

Methyl tetrahydro-4-oxo-2H-thiaran-3-carboxylic acid is a carboxylic acid ester derivative that can be used as an organic intermediate.

Chemical Properties

Light pink liquid

Synthesis

4131-74-2

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-CARBOXYLATESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Email
sales@accelachem.com
skychemical Co.Ltd
Tel
021-20958197 20965099
Email
sales@skychemical.com
Atop-Pharma (Shanghai) Technology Co., Ltd.
Tel
+86 (21) 5196-9732