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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652661Generated: October 26, 2026

Sodium Chloride → 6,7-Dichloro-5-hydroxy-2-hydroxymethylbenzo[b]thiophene

https://huagongshe.com/reaction/652661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium borohydrideHCID 4311764—
Reactant6,7-Dichloro-2-formyl-5-hydroxybenzo[b]thiopheneHCID 13290037—
SolventEthanolHCID 702—
Product6,7-Dichloro-5-hydroxy-2-hydroxymethylbenzo[b]thiopheneHCID 1329003874.4%

Reaction Steps

To a solution of 6.0 g of 6,7-dichloro-2-formyl-5-hydroxybenzo[b]thiophene and 300 ml of 90% ethanol is added portionwise 1.5 g of sodium borohydride. The reaction mixture is stirred at room temperature for 20 min. Saturated sodium chloride solution is added and the mixture is extracted three times with ethyl acetate:ether (1:1). The combined organic extracts are washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated to give 4.5 g of 6,7-dichloro-5-hydroxy-2-hydroxymethylbenzo[b]thiophene, mp 167°-169°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04672138
Source datasetuspto-grants-1987_06
ORD IDord-446f0d206f0d48bab133e3420746b254
Source noteuspto-grants-1987_06