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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307222Generated: November 2, 2026

Methanesulfonyl chloride → HCID 22605405, compound

https://huagongshe.com/reaction/2307222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 53767266HCID 53767266—
SolventDichloromethaneHCID 6344—
ProductHCID 22605405HCID 22605405—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-(4-fluorophenyl)-1-diphenylmethyl-3-azetidinol (15) (4.0 g) and N,N-diisopropylethylamine (3.2 mL) in dichloromethane (100 mL) at 0° C. was added, dropwise, methanesulfonyl chloride (125 mL). The mixture was stirred at 0° C. for 18 hrs, then washed (water, brine) and dried (Na2SO4) and concentrated in vacuo. The crude product was recrystallised from hexane to give 3-(4-fluorophenyl)-3-chloro-1-(diphenylmethyl)azetidine (16) (22 g), m.p. 108-109° C. (hexane). Found: C, 75.13; H, 5.46; N, 3.93. C22H19CIFN C, 75.10; H, 5.44; N, 3.98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831078B1
Source datasetuspto-grants-2004_12
ORD IDord-bafba58ab5c640f4b9df5d0192c1a98e
Source noteuspto-grants-2004_12