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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110373Generated: October 26, 2026

Potassium hydride → HCID 68904417, compound

https://huagongshe.com/reaction/2110373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydrideHCID 82127—
Reactant((2R,3R)-3-phenyloxiran-2-yl)methanolHCID 150502—
Reactant5-Fluoro-3-methyl-1H-indoleHCID 22351503—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
ProductHCID 68904417HCID 68904417—

Reaction Steps

A mixture of 5-fluoro-3-methyl-1H-indole (2.91 g, 19.5 mmol) and potassium hydride 50% dispersion in mineral oil (2.8 g, 35.1 mmol) in dichloromethane (40 mL) was stirred for 10 minutes under nitrogen at room temperature. A solution of [(2R,3R)-3-phenyloxiran-2-yl]methanol (2.0 g, 13.0 mmol) and titanium isopropoxide (4.3 mL, 14.3 mmol) in dichloromethane (10 mL) was then added and the mixture was stirred at room temperature for 12 hours. After disappearance of the epoxide, the mixture was partitioned between a 1 N aqueous solution of hydrochloric acid (50 mL) and ethyl acetate (50 mL). The organic layer was separated, washed with saturated sodium bicarbonate (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product was purified via Biotage chromatography (FlasH40i, silica, 60% ethyl acetate/hexane) to give (2S,3S)-3-(5-fluoro-3-methyl-1H-indol-1-yl)-3-phenyl propane-1,2-diol. MS (ES I) m/z 300

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517899B2
Source datasetuspto-grants-2009_04
ORD IDord-a3aa4f10b9a4411b9ab5bef3d362140d
Source noteuspto-grants-2009_04