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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198224Generated: November 4, 2026

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

https://huagongshe.com/reaction/1198224

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 53833740—

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 of (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280032
Source datasetuspto-grants-1994_01
ORD IDord-15ee4d60fc654426afbf0c5f0f09a5bf
Source noteuspto-grants-1994_01