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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508366Generated: October 24, 2026

Water → Ethyl 6-bromo-1-benzothiophene-2-carboxylate

https://huagongshe.com/en/reaction/508366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthyl ThioglycolateHCID 12185—
Reactant4-Bromo-2-fluorobenzaldehydeHCID 143517—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 6-bromo-1-benzothiophene-2-carboxylateHCID 13567982—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-bromo-2-fluorobenzaldehyde (1.02 g, 4.83 mmol) in DMSO (4 mL), was added ethyl 2-mercaptoacetate (0.58 mL, 5.31 mmol), followed by Et3N (1.35 mL, 9.65 mmol), and the mixture was heated at 80° C. for 3 h. The resulting dark mixture was poured into water (50 mL) and extracted with EtOAc (2×50 mL). The combined organic extracts were washed with 10% NaCl, dried over anhydrous Na2SO4, filtered and concentrated in vacuo to give the title compound as a light yellow waxy solid (1.29 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095590B2
Source datasetuspto-grants-2015_08
ORD IDord-2bd1c3a2130d4b158e0c21c2c5a54b5d
Source noteuspto-grants-2015_08