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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732047Generated: October 30, 2026

Triethylamine → Methanesulfonic acid 1-[5-(3-Chloro-phenyl)-isoxazol-3-yl]-ethyl ester

https://huagongshe.com/reaction/732047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57528604HCID 57528604—
SolventDichloromethaneHCID 6344—
ProductMethanesulfonic acid 1-[5-(3-Chloro-phenyl)-isoxazol-3-yl]-ethyl esterHCID 58812362—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a screw cap vial equipped with stir bar was added 1-[5-(3-chloro-phenyl)-isoxazole-3-yl]-ethanol (10 mg, 0.49 mmol), dichloromethane (3 ml) and triethylamine (0.34 ml, 2.46 mmol). Cooled the mixture down to 0° C. and to it added methane sulfonyl chloride (0.08 ml, 0.98 mmol). Left the reaction mixture stirring at room temperature for 30 min. Reaction was quenched with saturated sodium bicarbonate (aqueous, 40 ml) and extracted with dichloromethane (3×30 ml). Combined organic phase was washed with brine (40 ml), dried (sodium sulfate), filtered and concentrated, in-vacuo to isolate the desired compound as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-1b966cefb1ac49b782b6b8ea6654dc62
Source noteuspto-grants-2009_09