Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183643Generated: October 29, 2026

Hydrochloric Acid → 1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one

https://huagongshe.com/reaction/2183643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamideHCID 22473892—
ReactantHCID 178455855HCID 178455855—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-oneHCID 22473690—

Reaction Steps

Propylmagnesium chloride (2M solution in ether; 4.3 ml) was added under nitrogen over 15 minutes to a stirred solution of 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide (2 g) in tetrahydrofuran (25 ml) then the mixture was stirred at ambient temperature for 2.33 hours. Further propylmagnesium chloride (2M solution in ether; 0.5 ml) was added, the mixture was stirred at ambient temperature for 0.5 hours, then water (150 ml) and 5M hydrochloric acid (15 ml) were added. The product was extracted into dichloromethane (3×40 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified by column chromatography over silica using dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to leave 1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one (0.95 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-5cc97c0fdbce4ef689ec890feda21870
Source noteuspto-grants-2005_05