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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273135Generated: October 30, 2026

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

https://huagongshe.com/reaction/273135

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)-isoxazol-3-yl]-ethanol (110 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 numberUS07456200B2
Source datasetuspto-grants-2008_11
ORD IDord-6bf20a55beb241c79821c8b2e059208d
Source noteuspto-grants-2008_11