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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396859Generated: October 30, 2026

Sodium hydride → HCID 53768752, compound

https://huagongshe.com/reaction/2396859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(R)-1,2-EpoxypropaneHCID 146261—
ReactantHCID 18986280HCID 18986280—
SolventDiphenyl EtherHCID 7583—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53768752HCID 5376875279%

Reaction Steps

A suspension of 1.16 g of 6-chloro-5-fluoro-3-ethyl-indole-2-carboxylic acid in 16 ml of diphenyl ether was stirred at 260° for 4 hours and, after cooling to 0°, diluted with 24 ml of tetrahydrofuran. 180 mg of sodium hydride dispersion were added and the mixture was stirred for one hour. Subsequently, 0.5 ml of (R)-methyloxirane was added and the reaction mixture was stirred at room temperature for 112 hours. The mixture was extracted with diethyl ether, water and saturated sodium chloride solution and the organic phase was dried over sodium sulfate. The solvent was removed and the residue was chromatographed over 120 g of silica gel with hexane-toluene (1:2) and subsequently with toluene-ethyl acetate (9:1). 0.97 g (79%) of (R)-1-(6-chloro-5-fluoro-3-ethylindol-1-yl)-propan-2-ol was obtained as pale brown crystals with m.p. 112°-114°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494928
Source datasetuspto-grants-1996_02
ORD IDord-c4fb9909f334488d9070920e6180fce5
Source noteuspto-grants-1996_02