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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649003Generated: October 26, 2026

N-bromobutanimide → 7-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/649003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Methyl-1-benzothiopheneHCID 6428541—
SolventCarbon TetrachlorideHCID 5943—
Product7-(Bromomethyl)-1-benzothiopheneHCID 10751761—

Reaction Steps

7 g of 7-methylbenzo[b]thiophene, 8,5 g of N-bromosuccinimide and a spatula tip of α,α'-azoisobutyronitrile are refluxed together for 6 hours in 50 ml of carbon tetrachloride. The resulting mixture is cooled, filtered and concentrated by evaporation. The resulting raw title compound can be directly employed in the next step. M.p. when isolated=57° (isopropanol)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737516
Source datasetuspto-grants-1988_04
ORD IDord-b271bc6775614609b28f0c5fa1cee288
Source noteuspto-grants-1988_04