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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870047Generated: October 30, 2026

3-Chlorobenzaldehyde → (4-Bromo-2,5-dichloro-3-thienyl)(3-chlorophenyl)methanol

https://huagongshe.com/reaction/870047

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzaldehydeHCID 11477—
Reactant3,4-Dibromo-2,5-dichlorothiopheneHCID 7015318—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-2,5-dichloro-3-thienyl)(3-chlorophenyl)methanolHCID 57900988—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3,4-dibromo-2,5-dichlorothiophene (2.00 g, 6.43 mmol) in THF (18 mL) at −78° C., was added n-BuLi (2.5M in hexane, 2.57 mL, 6.43 mmol) dropwise. After 30 min., 3-chlorobenzaldehyde (0.732 mL, 6.43 mmol) was added dropwise to the yellow solution. The resulting solution was stirred at −78° C. for 30 min. and allowed to warm to 0° C. After 30 min., the reaction was quenched by the addition of 25% aq. NH4OAc. The aqueous layer was extracted with EtOAc and the combined organics were washed with water and brine, dried (Na2SO4) and concentrated. The crude product was purified by chromatography on silica gel (50:50 to 80:20 CHCl3/hexane) to afford the desired product as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969394B2
Source datasetuspto-grants-2015_03
ORD IDord-5ec3e8f4ff7345f4b17b6326447c023e
Source noteuspto-grants-2015_03