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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485890Generated: October 25, 2026

Hydrochloric Acid → 2-Acetyl-6,7-dichloro-5-methoxybenzo[b]thiophene

https://huagongshe.com/reaction/485890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant6,7-Dichloro-5-methoxybenzo[b]thiopheneHCID 13289996—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-Acetyl-6,7-dichloro-5-methoxybenzo[b]thiopheneHCID 13952874—

Reaction Steps

To a solution of 5.0 g of 6,7-dichloro-5-methoxybenzo[b]thiophene in 30 ml of dry tetrahydrofuran and 10 ml dry ethyl ether under nitrogen at -20° is added 11.7 ml of 2.2M n-butyllithium, while the temperature is maintained at -20°. After stirring for 2 hours at this temperature, the reaction mixture is added dropwise through a transfer needle to a stirred solution of 22 ml of freshly distilled acetic anhydride in 40 ml of dry tetrahydrofuran at -20°. Five minutes after the addition, the reaction mixture is poured onto 100 ml 10% hydrochloric acid. The mixture is extracted twice with dichloromethane, the organic layers are collected and dried and the solvent is removed to give a solid. The solid is washed with ethyl ether to give 1.5 g of 2-acetyl-6,7-dichloro-5-methoxybenzo[b]thiophene as a fluffy solid. Recrystallization of the residue obtained by evaporation of the filtrate from ethyl ether-hexane gives an additional 0.6 g of 2-acetyl-6,7-dichloro-5-methoxybenzo[b]thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537976
Source datasetuspto-grants-1985_08
ORD IDord-5d2fdda7a8d8484aa4f12b4d4f14f2ad
Source noteuspto-grants-1985_08