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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739715Generated: October 26, 2026

Water → 3-Bromobenzo[b]thiophene-5-carboxaldehyde

https://huagongshe.com/reaction/1739715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantBromineHCID 24408—
ReactantBenzo(b)thiophene-5-carboxaldehydeHCID 139097—
SolventAcetic AcidHCID 176—
Product3-Bromobenzo[b]thiophene-5-carboxaldehydeHCID 18691608—

Reaction Steps

To a solution of 3 g of benzo[b]thiophene-5-carbaldehyde in 30 ml of acetic acid is dropwise added 1.43 ml of bromine with ice-cooling. The temperature of the reaction mixture is elevated to room temperature, at which temperature the mixture is stirred for three hours. After the reaction, 50 ml of water and 50 ml of ethyl acetate are added to the thus stirred reaction mixture, and the resulting organic layer was separated, washed successively with water, a saturated aqueous sodium hydrogencarbonate solution and a saturated saline solution and then dried over anhydrous magnesium sulfate. Thereafter, the solvent is removed from the thus dried layer by distillation under reduced pressure. The residue obtained is purified by a moderate pressure column chromatography [eluent:hexane:ethyl acetate=20:1], to obtain 4.2 g of 3-bromobenzo[b]thiophene-5-carbaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968935
Source datasetuspto-grants-1999_10
ORD IDord-a3d322f1966344cdb4aa6da3a4cf74fe
Source noteuspto-grants-1999_10