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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35537Generated: October 28, 2026

Acetic Acid → 3-Acetoxy-2-(4-methoxyphenyl)-6-azabenzo[b]thiophene

https://huagongshe.com/reaction/35537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-(4-methoxyphenyl)methylthiopyridine-4-carboxylateHCID 86742397—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-Acetoxy-2-(4-methoxyphenyl)-6-azabenzo[b]thiopheneHCID 1427763848%

Reaction Steps

A solution of 0.200 g (.69 mmol) of methyl 3-(4-methoxyphenyl)methylthiopyridine-4-carboxylate in 2 mL of dry tetrahydrofuran was added to a suspension of 83 mg (2.1 mmol) of 60% dispersion of sodium hydride in 2 mL of dry N,N-dimethylformamide. The mixture was stirred at room temperature for 3 hours, then poured onto ice water and acidified with glacial acetic acid. The solid material (product) was collected by filtration and the filtrate was extracted with ethyl acetate. The ethyl acetate extract was dried, concentrated and combined with the solid precipitate that had been collected. This material was heated at reflux with 100 mg sodium acetate in 2 mL of acetic anhydride for 2 hours, then was partitioned between ethyl acetate and water. The aqueous layer was washed with two portions of ethyl acetate and the combined extracts were dried and concentrated. The residue was crystallized from methanol to afford 100 mg (48%) of white crystalline material, m.p. 141-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767766
Source datasetuspto-grants-1988_08
ORD IDord-8f4e2abc12d546a996287a3be0ac6dcc
Source noteuspto-grants-1988_08