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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747182Generated: October 30, 2026

Triethylamine → [3-(4-Bromophenyl)-4,5-dihydroisoxazol-5-yl]methyl methanesulfonate

https://huagongshe.com/reaction/747182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant[3-(4-Bromophenyl)-4,5-dihydro-1,2-oxazol-5-yl]methanolHCID 15888252—
SolventDichloromethaneHCID 6344—
Product[3-(4-Bromophenyl)-4,5-dihydroisoxazol-5-yl]methyl methanesulfonateHCID 18698757100.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

[3-(4-Bromo-phenyl)-4,5-dihydro-isoxazol-5-yl]-methanol (84.3 g, 328 mmol) was added to anhydrous dichloromethane (500 ml) followed by addition of triethylamine (64.1 ml, 459.2 mmol). The solution was allowed to cool to 0° C. followed by dropwise addition of methane sulfonyl chloride (30.65 ml, 396 mmol). The reaction was stirred for 2 hours at 0° C. and then aqueous sodium bicarbonate (200 ml) was added. After further extraction with dichloromethane (2×200 ml), the organic layers were combined, dried over sodium sulfate, and concentrated in vacuo to give the desired product (110 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396847B2
Source datasetuspto-grants-2008_07
ORD IDord-5de72995025d4967b05cf58a32c86df7
Source noteuspto-grants-2008_07