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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380789Generated: November 3, 2026

Water → Methyl 3-amino-5-phenylthiophene-2-carboxylate

https://huagongshe.com/reaction/2380789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl ThioglycolateHCID 16907—
Reactant3-Chloro-3-phenyl-2-propenenitrileHCID 2777511—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 70056262.9%

Reaction Steps

To a solution of methyl thioglycolate (1 g, 9.43 mmol) in methanol (5 mL) was added a solution of sodium methoxide (0.5 g, 9.43 mmol) in methanol (5 mL) and stirred for 0.5 h. To the above mixture, a solution of 3-chloro-3-phenylprop-2-enenitrile (1.22 g, 7.5 mmol) in DMF (3.5 mL) was added dropwise for 10 min at rt and stirred the mixture at 60° C. for 2 h. Then, a solution of sodium methoxide (1 g, 18.6 mmol) in methanol (10 mL) was added dropwise at rt and stirring was continued for 2 h at 60° C. The mixture was allowed to rt and poured into cold water and stirred for 15 min. The solution was extracted with chloroform (3×100 mL) and the combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel using hexane-ethyl acetate (92:8) as eluent to give the product as a pale yellow color solid (1.1 g, 50%), mp 130-132° C. 1H NMR (400 MHz, DMSO-d6): δ 7.62-7.65 (2H, m), 7.38-7.48 (3H, m), 7.00 (1H, s), 4.29 (2H, br s), 3.74 (3H, s); LC-MS (positive ion mode): m/z 234 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258119B2
Source datasetuspto-grants-2012_09
ORD IDord-9b488cadbbca4e889ff9f28a4ab35be6
Source noteuspto-grants-2012_09