Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581736Generated: October 31, 2026

Water → 2-(2-Chloroethoxy)-1-(6-fluorobenzo[b]thiophen-5-yl)ethanol

https://huagongshe.com/reaction/581736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoraneHCID 6331—
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
Reactant2-(2-Chloroethoxy)-1-(6-fluorobenzo[b]thiophen-5-yl)ethanoneHCID 18691600—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(2-Chloroethoxy)-1-(6-fluorobenzo[b]thiophen-5-yl)ethanolHCID 1540858099.3%

Reaction Steps

To a solution of 4.5 g of 2-(2-chloroethoxy)-1-(6-fluorobenzo[b]thiophen-5-yl)ethanone in 45 ml of tetrahydrofuran is added 0.46 g of (R)-5,5-diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine at -10° C., and thereafter, 9.9 ml of 1 M borane solution of tetrahydrofuran is dropwise added thereto. The temperature of the resulting mixture is elevated to room temperature, and the mixture is stirred at the same temperature for 1.5 hours, after which 100 ml of water and 100 ml of ethyl acetate are added thereto. The resulting organic layer is separated, washed successively with water and a saturated saline solution and then dried over anhydrous magnesium sulfate. The solvent is then removed from the thus dried layer by distillation under reduced pressure. The residue obtained is purified by a column chromatography [eluent:toluene:ethyl acetate=10:1], to obtain 4.5 g of oily (+)-2-(2-chloroethoxy)-1-(6-fluoro-benzo[b]thiophen-5-yl)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922721
Source datasetuspto-grants-1999_07
ORD IDord-ce4d4a87b0fd4179b065f9d681a413f4
Source noteuspto-grants-1999_07