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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822973Generated: October 31, 2026

Hydrochloric Acid → 4-Cyano-7-hydroxy benzo[b]thiophene

https://huagongshe.com/reaction/1822973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantSodium ethanethiolateHCID 4459711—
Reactant4-Cyano-7-methoxy benzo[b]thiopheneHCID 22171123—
SolventDimethylformamideHCID 6228—
Product4-Cyano-7-hydroxy benzo[b]thiopheneHCID 2217118999.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 4-cyano-7-methoxy benzo[b]thiophene (450 mg, 2.38 mmol, 1 equiv.) in dry DMF (20 mL) was added sodium ethanethiolate (80% technical grade, 1.34 g, ˜13 mmol, ˜5 equiv.) and the reaction mixture was heated at 150° C. for 2 hr. The mixture was cooled to room temperature and ethyl acetate and 1N HCl were added and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic extracts were washed with brine (3 times), dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The acquired material thus obtained was purified via medium pressure liquid chromatography eluting with 30% ethyl acetate/70% hexanes to afford the title compound (414 mg, 99%) as a colorless solid; □H (400 MHz, CD3OD) 6.80 (1H, d, J=8 Hz), 7.47 (1H, d, J=6 Hz), 7.64 (1H, d, J=8 Hz), 7.83 (1H, d, J=6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037932B2
Source datasetuspto-grants-2006_05
ORD IDord-e55a3dc0c97448aab0497a7a63ac9f13
Source noteuspto-grants-2006_05