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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396853Generated: October 29, 2026

Water → 1H-Indole-1-ethanol, 5-chloro-6-fluoro-α-methyl-, (R)-

https://huagongshe.com/reaction/2396853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(R)-1,2-EpoxypropaneHCID 146261—
Reactant5-chloro-6-fluoro-1H-indoleHCID 2773647—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1H-Indole-1-ethanol, 5-chloro-6-fluoro-α-methyl-, (R)-HCID 5378859977%

Reaction Steps

A suspension of 128 mg of sodium hydride dispersion in 8 ml of tetrahydrofuran was treated with 0.5 7 g of 5-chloro-6-fluoroindole at 0° and stirred at this temperature for 1 hour. After the addition of 0.48 ml of (R)-methyloxirane the reaction mixture was stirred at room temperature for 48 hours and subsequently treated with water. The mixture was diluted with ether, washed with water and with saturated sodium chloride solution and the organic phase was dried over sodium sulfate. After removing the solvent the residue was chromatographed over 25 g of silica gel with toluene-ethyl acetate (19:1). There was obtained 0.59 g (77%) of (R)-1-(5-chloro-6-fluoro-indol-1-yl)-propan-2-ol as beige crystals with m.p. 108°-110°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494928
Source datasetuspto-grants-1996_02
ORD IDord-65ff0a26b5ae4fd68dc085ecf1ca3e51
Source noteuspto-grants-1996_02