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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183616Generated: November 1, 2026

Hydrochloric Acid → 1-(4-Chlorobenzo[b]thien-2-yl)-1-propanone

https://huagongshe.com/reaction/2183616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamideHCID 22473892—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chlorobenzo[b]thien-2-yl)-1-propanoneHCID 22473854—

Reaction Steps

Ethylmagnesium bromide (1M solution in tetrahydrofuran; 17.2 ml) was added under nitrogen to a stirred solution of 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide (4 g; prepared in a manner similar to that described in Example 18) in tetrahydrofuran (120 ml) then the mixture was allowed to stand at ambient temperature for 30 minutes, heated under reflux for 30 minutes and allowed to stand at ambient temperature for 30 minutes. Further ethylmagnesium bromide (1M solution in tetrahydrofuran; 7.0 ml) was added and the mixture was allowed to stand at ambient temperature for 2 hours. Water (200 ml) and 5M hydrochloric acid (15 ml) were added, and the product was extracted into dichloromethane (2×90 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)propan-1-one (1.88 g) as a pale yellow solid, m.p. 96-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-0aaab9e0289b4dac8374d955fd4f678b
Source noteuspto-grants-2005_05