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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584157Generated: October 31, 2026

Triethylamine → HCID 131725059, compound

https://huagongshe.com/reaction/584157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86759793HCID 86759793—
SolventDichloromethaneHCID 6344—
ProductHCID 131725059HCID 13172505997.8%

Reaction Steps

A solution of (3R and 3S)-1-[4-(3-hydroxypropyl)phenoxy]-3-[4-(tert-butoxycarbonyl)phenoxy]-2-butanone (1.57 g, 3.8 mmol) in dry dichloromethane (25 ml) was cooled to 0-50° C. and treated with triethylamine (1.1 ml, 7.9 mmol) followed by methanesulfonyl chloride (0.5 mL, 6.46 mmol) added dropwise over 2 minutes. After 45 minutes at 0-5° C., the reaction mixture was quenched by addition of ethyl acetate and saturated sodium bicarbonate. The organic phase was washed with brine and dried (anhydrous magnesium sulfate) and evaporated. Chromatography of the residual oil on silica gel (elution toluene-ethyl acetate, 9:1) gave 1.83 g (97%) of the title material as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924391B2
Source datasetuspto-grants-2005_08
ORD IDord-3fa81723c91649589764495e77b9d56b
Source noteuspto-grants-2005_08