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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519238Generated: October 30, 2026

Methanesulfonyl chloride → 1-Benzhydryl-3-methylazetidin-3-yl methanesulfonate

https://huagongshe.com/reaction/519238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Benzhydryl-3-methylazetidin-3-olHCID 10243989—
SolventDichloromethaneHCID 6344—
Product1-Benzhydryl-3-methylazetidin-3-yl methanesulfonateHCID 1006529598.4%

Reaction Steps

To a 0° C. solution of 1-benzhydryl-3-methylazetidin-3-ol (70 g, 276 mmol) and TEA (53.1 g, 525 mmol) in DCM (700 mL) was added drop-wise methanesulfonyl chloride (57 g, 497 mmol). The reaction mixture was stirred for 2 h then filtered and the filter cake was washed with DCM (3×50 mL). The filtrate was washed with water (3×100 mL), dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo to give methanesulfonic acid 1-benzhydryl-3-methyl-azetidin-3-yl ester (90 g, 98%) as a brown solid, which was used in the next step without further purification. 1H NMR (CDCl3, 400 MHz): δ 7.44 (m, 4H), 7.33 (m, 4H), 7.26 (m, 2H), 4.55 (brs, 1H), 3.46 (m, 4H), 3.07 (s, 3H), 1.94 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-f93d10d142704277b972e01cb36e3aa0
Source noteuspto-grants-2015_08