ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE
ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Basic information
- Product Name:
- ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE
- Synonyms:
-
- RARECHEM AL BI 0303
- Ethyl 5-chloro-2-thiophenecarboxylate
- 5-Chlorothiophene-2-carboxylic acid ethyl ester
- Ethyl 5-chlorothiophene-2-carboxlate
- Ethyl 5-chlorothiophene-2-carboxylate, 98+%
- 2-Thiophenecarboxylic acid, 5-chloro-, ethyl ester
- 2- chlorinethiophene -5-ethyl forMate
- Rivaroxaban impurity P2-O
- CAS:
- 5751-82-6
- MF:
- C7H7ClO2S
- MW:
- 190.65
- Mol File:
- 5751-82-6.mol
ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Chemical Properties
- Boiling point:
- 70-71°C 1mm
- Density
- 1.312±0.06 g/cm3(Predicted)
- refractive index
- 1.5380
- Flash point:
- 70-71°C/1mm
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- form
- clear liquid
- color
- Colorless to Light yellow
- BRN
- 128707
- CAS DataBase Reference
- 5751-82-6
MSDS
- Language:English Provider:ALFA
ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Usage And Synthesis
Chemical Properties
Colorless to light yellow liquid
Synthesis
24065-33-6
64-17-5
5751-82-6
Concentrated sulfuric acid (15 mL) was slowly added to a stirring solution of 5-chlorothiophene-2-carboxylic acid (15 g, 0.0925 mol) in ethanol (300 mL) at room temperature. The reaction mixture was stirred continuously under anhydrous conditions for 16 hours. Upon completion of the reaction, the reaction mixture was concentrated by distillation under reduced pressure. The concentrate was diluted with ethyl acetate (300 mL) and the organic layer was subsequently washed sequentially with water (3 x 100 mL), saturated sodium bicarbonate solution (3 x 100 mL) and saturated saline (100 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give ethyl 5-chlorothiophene-2-carboxylate (14 g, 80% yield) as a colorless liquid.
References
[1] Patent: WO2015/18534, 2015, A1. Location in patent: Page/Page column 39
[2] Journal of the American Chemical Society, 1954, vol. 76, p. 5131
[3] Journal of the American Chemical Society, 1954, vol. 76, p. 5131
[4] Chemistry - A European Journal, 2016, vol. 22, # 1, p. 211 - 221
ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Preparation Products And Raw materials
Raw materials
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ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE(5751-82-6)Related Product Information
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- ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE
- 2-Chloro-5-thiophenecarboxaldehyde
- 5-Chlorothiophene-2-ylmethanol
- 2-Thiophenecarboxylic acid hydrazide
- 2-Chloro-5-methylthiophene
- Ethyl 2-thiophenecarboxylate
- METHYL THIOPHENE-2-CARBOXYLATE