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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354085Generated: October 25, 2026

Hydrochloric Acid → 2-(4-Methoxyphenyl)-3-(4-Hydroxybenzoyl)-6-Methoxybenzo[b]thiophene

https://huagongshe.com/reaction/354085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanethiolHCID 6343—
ReactantLY88074 Trimethyl etherHCID 9953060—
ReactantButyllithiumHCID 178418339—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Methoxyphenyl)-3-(4-Hydroxybenzoyl)-6-Methoxybenzo[b]thiopheneHCID 9865197—

Reaction Steps

To a solution of ethanethiol (538 mL, 7.27 mmol) in 1.88 mL of tetrahydrofuran, cooled to −30° C. was added n-butyllithium (2.57 mL, 2.5 M, 6.42 mmol) and the reaction was warmed to room temperature. Dimethylformamide (1 mL) was added then the product from Step 1 (1.73 g, 4.3 mmol) in 2.7 mL of dimethylformamide. The reaction was heated at 58° C. for two hours then at 80° C. for 1 hour. The cooled reaction was poured into 33 mL oh 1N hydrochloric acid and extracted with ethyl acetate. The combined organic layers was washed with brine and dried over anhydrous magnesium sulfate. After filtration, concentration and silica gel column chromatography using 15% ethyl acetate -hexanes as eluant the title compound (1.17 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756388B1
Source datasetuspto-grants-2004_06
ORD IDord-833a6e54d2d04733b394359c809d7828
Source noteuspto-grants-2004_06