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Methyl 3-methylthiophene-2-carboxylate

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Methyl 3-methylthiophene-2-carboxylate manufacturers

Methyl 3-methylthiophene-2-carboxylate Basic information
Product Name:Methyl 3-methylthiophene-2-carboxylate
Synonyms:RARECHEM AL BF 0178;3-Methylthiophene-2-carboxylic acid methyl ester;Methyl 3-methylthiophene-2-carboxylate ,99%;3-Methylthiophene-2-Cabroxylate;Eethyl3-methylthiophene-2-carboxylate;3-methylthiophene-2-carboxylate;3-methyl-2-thiophenecarboxylic acid methyl ester;Methyl 3-Methylthiophene-2-carboxylate >
CAS:81452-54-2
MF:C7H8O2S
MW:156.2
EINECS:
Product Categories:
Mol File:81452-54-2.mol
Methyl 3-methylthiophene-2-carboxylate Structure
Methyl 3-methylthiophene-2-carboxylate Chemical Properties
Boiling point 216-217°C
density 1.173±0.06 g/cm3(Predicted)
refractive index 1.5168
Fp 216-217°C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow
BRN 116836
InChIInChI=1S/C7H8O2S/c1-5-3-4-10-6(5)7(8)9-2/h3-4H,1-2H3
InChIKeyBRWROFVPMUPMJQ-UHFFFAOYSA-N
SMILESC1(C(OC)=O)SC=CC=1C
Safety Information
Safety Statements 23-24/25
HS Code 29151300
MSDS Information
ProviderLanguage
ALFA English
Methyl 3-methylthiophene-2-carboxylate Usage And Synthesis
Chemical PropertiesColorless liquid
Synthesis
Methanol

67-56-1

3-Methyl-2-thiophenecarboxylic acid

23806-24-8

METHYL 3-METHYLTHIOPHENE-2-CARBOXYLATE

81452-54-2

Step 1: Synthesis of methyl 3-methylthiophene-2-carboxylate: 3-methylthiophene-2-carboxylic acid (15 g, 105 mmol, 1.0 eq.) was dissolved in methanol (150 mL) and concentrated sulfuric acid (7.5 mL) was added slowly and dropwise. The reaction mixture was heated to reflux for 12 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate (200 mL) and washed sequentially with water (2 x 50 mL), saturated aqueous sodium bicarbonate solution (2 x 50 mL) and brine (50 mL). The organic phase was dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to afford 20 g (97% yield) of methyl 3-methylthiophene-2-carboxylate as an oil. The product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.38 (d, J=5.0 Hz, 1H), 6.91 (d, J=5.0 Hz, 1H), 3.85 (s, 3H), 2.55 (s, 3H); ESI-MS m/z 157 ([M+H]+).

References[1] Patent: WO2012/56478, 2012, A1. Location in patent: Page/Page column 75-76
[2] Patent: WO2007/124546, 2007, A1. Location in patent: Page/Page column 58
[3] Patent: WO2014/64131, 2014, A2. Location in patent: Page/Page column 114; 115
[4] Patent: WO2014/76104, 2014, A1. Location in patent: Page/Page column 79-80
[5] Journal of Medicinal Chemistry, 1995, vol. 38, # 24, p. 4806 - 4820
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