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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584153Generated: October 31, 2026

Triethylamine → HCID 86759792, compound

https://huagongshe.com/reaction/584153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86759791HCID 86759791—
SolventDichloromethaneHCID 6344—
ProductHCID 86759792HCID 8675979283.1%

Reaction Steps

A solution of (3R and 3S)-3-[4-(3-hydroxypropyl)phenoxy]-1-[4-(tert-butoxycarbonyl)phenoxy]-2-butanone (0.092 g, 0.22 mmol) in dry dichloromethane (5 ml) was cooled to 0° C. and treated with triethylamine (0.07 ml, 0.5 mmol) followed by methanesulfonyl chloride (0.03 ml, 0.39 mmol). After 45 minutes at 0° C., the reaction mixture was quenched by addition of ethyl acetate (100 ml) and water. The organic phase was washed with saturated sodium bicarbonate, brine and dried (magnesium sulfate). Evaporation and chromatography of the residue on silica gel (elution toluene and ethyl acetate, 9:1) gave 0.090 g (82%) of the title material as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924391B2
Source datasetuspto-grants-2005_08
ORD IDord-f805600e393c4da386fdd7f67f6b0dcd
Source noteuspto-grants-2005_08