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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392497Generated: October 26, 2026

Triethylamine → (1-Benzhydrylazetidin-3-yl)methyl methanesulfonate

https://huagongshe.com/reaction/392497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(1-Benzhydrylazetidin-3-yl)methanolHCID 2758715—
SolventDichloromethaneHCID 6344—
Product(1-Benzhydrylazetidin-3-yl)methyl methanesulfonateHCID 2197837099%

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound from Step B above (1.7 g, 6.72 mmoles) and triethylamine (1.1 g, 10.87 mmoles) were dissolved in CH2Cl2 (20 mL) and the mixture was stirred under nitrogen at 0° C. Methanesulfonylchloride (1.1 g, 9.6 mmoles) was added and the solution was stirred at room temperature for 2 h. The solution was diluted with CH2Cl2 and washed with saturated aqueous sodium bicarbonate, water and dried (MgSO4), filtered and evaporated to dryness to give the title compound (2.32 g, 99%). FABMS (M+1)=332.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800636B2
Source datasetuspto-grants-2004_10
ORD IDord-be4167c7ed454984976d4cd793f7cd00
Source noteuspto-grants-2004_10