Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081965Generated: October 27, 2026

N-methoxycarbonyl-N-phenyl-7-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-6-carboxylic acid methyl ester → 4,5-Dihydrobenzo[b]thiophene-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/1081965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methoxycarbonyl-N-phenyl-7-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-6-carboxylic acid methyl esterHCID 15389403—
SolventMethanolHCID 887—
SolventSodium MethoxideHCID 10942334—
Product4,5-Dihydrobenzo[b]thiophene-6-carboxylic acid methyl esterHCID 1051201782.9%

Reaction Steps

N-methoxycarbonyl-N-phenyl-7-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-6-carboxylic acid methyl ester (100 mg, 0.290 mmol) was dissolved in methanol (3 ml), to which sodium methoxide (28% methanol solution, 1 ml) was added and stirred at room temperature overnight. The reaction mixture was poured into ice water and extracted with diethyl ether. After washing the liquid extract with an aqueous solution of sodium chloride and drying over sodium sulfate, the solvent was distilled off. The residue was purified by silica gel column chromatography to obtain 46.7 mg (yield 48%) of 4,5-dihydrobenzo[b]thiophene-6-carboxylic acid methyl ester as white crystalline solids. 1H-NMR spectra (chemical shift, ppm: in CDCl3): 2.68 (2H, m), 2.84 (2H, m), 3.79 (3H, s), 6.90 (1H, d, J=4.9 Hz), 7.31 (1H, d, J=4.9 Hz), 7.53 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587486
Source datasetuspto-grants-1996_12
ORD IDord-684102a2b72b46de8548ca9abcd75538
Source noteuspto-grants-1996_12