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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783971Generated: October 29, 2026

Diethyl Carbonate → Ethyl benzo[b]thiophene-7-carboxylate

https://huagongshe.com/reaction/1783971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl CarbonateHCID 7766—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant7-Bromobenzo[b]thiopheneHCID 12045538—
SolventTetrahydrofuranHCID 8028—
ProductEthyl benzo[b]thiophene-7-carboxylateHCID 4975802371%

Reaction Steps

7-bromobenzo[b]thiophene (500 mg, 2.36 mmol) is dissolved in dry THF (5.0 mL) under nitrogen. Magnesium turnings (530 mg, 2.83 mmol, 1.20 equiv.) are added and the resulting mixture is heated at reflux until dissolution of the magnesium has occurred. The resulting cloudy yellow solution is allowed to cool to rt and diethyl carbonate (2 mL, excess) is added and stirring continued for one hour, when ammonium chloride (10% aq) is added. The resulting mixture is partitioned between DCM and water and the aqueous layer is extracted with DCM. The organic fractions are combined, washed with brine, dried over Na2SO4 and adsorbed onto silica. Purification by LC using 8/2 cyclohexane/dichloromethane as the eluent afforded the title compound as a pale orange oil (346.2 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501411B2
Source datasetuspto-grants-2009_03
ORD IDord-8557a574f6614ac88eef6422d26425a2
Source noteuspto-grants-2009_03