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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523546Generated: November 3, 2026

Diisopropylamine → 5-Bromo-2-chlorobenzo[b]thiophene

https://huagongshe.com/reaction/523546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant5-Bromo-1-benzothiopheneHCID 2776578—
ReactantN-chlorosuccinamideHCID 15238416—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Bromo-2-chlorobenzo[b]thiopheneHCID 1854246630.1%

Reaction Conditions

Temperature-20 °C

Reaction Steps

n-Butyl lithium (0.64 ml, 1.2 mmol) was added drop wise to a solution of diisopropyl amine (0.25 mL, 1.5 mmol) in dry THF at −78° C. under nitrogen atmosphere over a period of 5 minutes. The reaction mixture was stirred at −20° C. for 30 minutes. To this was added 5-bromo-benzo[b]thiophene (200 mg, 0.938 mmol) in dry THF at −78° C., continued stirring for a further 30 minutes at −78° C., followed by the addition of N-chlorosuccinamide (225 mg, 1.68 mmol) in dry THF at −78° C. The resulting mixture was stirred at room temperature for 2 hours. The reaction was monitored by TLC (100% hexane). The reaction mixture was partitioned between ethyl acetate and saturated ammonium chloride. The organic layer was dried over sodium sulfate and concentrated to afford the crude product. Purification by column chromatography on silica gel (100% hexane) afforded 70 mg of the product (30% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339501B2
Source datasetuspto-grants-2016_05
ORD IDord-3ec49e29adc9421a8d966f6549417200
Source noteuspto-grants-2016_05