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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413584Generated: October 25, 2026

Hydrochloric Acid → Ethyl 2,3-dihydro-1-benzothiepine-4-carboxylate

https://huagongshe.com/reaction/413584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-(2-formylphenylthio)butyrateHCID 18533389—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2,3-dihydro-1-benzothiepine-4-carboxylateHCID 1148171944%
Product2,3-Dihydro-1-benzothiepine-4-carboxylic acidHCID 178242476.4%

Reaction Steps

Ethyl 4-(2-formylphenylthio)butyrate (537 mg) was dissolved in 6 ml of tetrahydrofuran and a suspension of 60% sodium hydride (102 mg) in 5 ml of tetrahydrofuran was dropped at room temperature. Stirring was conducted at room temperature for 1 hour. The mixture was stirred for 30 minutes under reflux. During cooling in ice, 4 ml of a 1N hydrochloric acid was added. Extraction with 10 ml of ethyl acetate was conducted. The organic layer was washed with 20 ml of water three times. The quantitative analysis by HPLC found 220 mg (Yield 44%) of ethyl 2,3-dihydro-1-benzothiepine-4-carboxylate and 28 mg (Yield 6.4%) of 2,3-dihydro-1-benzothiepine-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566535B1
Source datasetuspto-grants-2003_05
ORD IDord-e31508c8d36740e19adee23e301de278
Source noteuspto-grants-2003_05