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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915873Generated: October 31, 2026

Triethylamine → Oxetan-3-ylmethyl methanesulfonate

https://huagongshe.com/reaction/1915873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantOxetan-3-ylmethanolHCID 11521066—
SolventDichloromethaneHCID 6344—
ProductOxetan-3-ylmethyl methanesulfonateHCID 86680078—

Reaction Conditions

Temperature0 °C

Reaction Steps

Oxetan-3-ylmethanol (1.85 g, 21.0 mmol) was dissolved in methylene chloride and cooled to 0° C. Triethylamine (5.31 g, 52.2 mmol) was added followed by slow addition of methanesulfonyl chloride (2.89 g, 25.2 mmol). The mixture was allowed to warm to ambient temperature for 2 h and quenched with sat. sodium bicarbonate (14 mL). The aqueous solution was extracted with methylene chloride 3×. The combined organic layers were dried over sodium sulfate, filtered and concentrated to give crude oxetan-3-ylmethyl methanesulfonate (quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614206B2
Source datasetuspto-grants-2013_12
ORD IDord-3452a4ced46a404d9ad0478512be16b4
Source noteuspto-grants-2013_12