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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121295Generated: October 25, 2026

2-Pentylthiophene → 2-bromo-5-pentylThiophene

https://huagongshe.com/reaction/2121295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PentylthiopheneHCID 20995—
ReactantN-bromobutanimideHCID 67184—
ReactantAcetic acid chloroformHCID 21584526—
SolventWaterHCID 962—
Product2-bromo-5-pentylThiopheneHCID 1131082597.6%

Reaction Steps

A solution of 2-pentylthiophene, (25.2 g) N-bromosuccinimide (25.5 g) and a 1:1 chloroform acetic acid mixture (100 cm3) was heated under reflux for 1 h. Water (10 cm3) was added and the resultant solution stirred for 10 min under an atmosphere of nitrogen. The organic layer was separated off and the aqueous layer extracted with diethyl ether (2×50 cm3). The combined organic layers were washed with brine (2×100 cm3), dried (MgSO4), filtered and then evaporated down. The residue was purified by distillation (Bp 132-134° C. at 15-20 mm Hg.) to yield 32.6 g of 2-bromo-5-pentylthiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696110B1
Source datasetuspto-grants-2004_02
ORD IDord-76bad079f71b44409d06f5ec6a1ec022
Source noteuspto-grants-2004_02