Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259343Generated: November 3, 2026

Ethyl Acetate → (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol

https://huagongshe.com/reaction/2259343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-(1-Benzothiophen-5-yl)-2-bromo-1-ethanoneHCID 7060546—
SolventTetrahydrofuranHCID 8028—
Product(R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanolHCID 5383374094.3%

Reaction Conditions

Temperature-25 °C

Reaction Steps

A solution of 7.5 g of (+)-diisopinocamphenylchloroborane dissolved in 15 ml of tetrahydrofuran was cooled to -25° C. Thereto was added 4 g of 5-bromoacetylbenzo[b]thiophene. The resulting mixture was stirred for 4 hours at -20° C. to -15° C. The reaction mixture was added to a mixture of 80 ml of ethyl acetate and 80 ml of ice water. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (eluant: hexane:ethyl acetate=10:1) to obtain 3.8 g of (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05472984
Source datasetuspto-grants-1995_12
ORD IDord-12418fdf7e0741ae97c656a9eb14fb53
Source noteuspto-grants-1995_12