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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051750Generated: November 1, 2026

Methanesulfonyl chloride → HCID 118103467, compound

https://huagongshe.com/reaction/1051750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-4-(2,4,5-trifluorophenyl)butanoic acidHCID 23146023—
SolventAcetonitrileHCID 6342—
ProductHCID 118103467HCID 11810346796.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To the rapidly stirred 80° C. suspension of methanesulfonyl chloride (0.88 g, 7.72 mmol) and sodium bicarbonate (3.24 g, 38.6 mmol) in acetonitrile (400 mL), 3-amino-4-(2,4,5-trifluorophenyl)butanoic acid ((±)-Ia, 1.5 g, 6.43 mmol) is added over period of 2 h. The resulting suspension was further stirred for 16 h at 80° C., after which time the fine suspension was cooled to 0° C. and filtered. The filtrate was evaporated under reduced pressure to afford 1.34 g (96% yield) of racemic 4-(2,4,5-trifluorobenzyl)azetidin-2-one ((±)-IIa) as pale yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388188B2
Source datasetuspto-grants-2016_07
ORD IDord-4ed0499a4ea74ce0a773a8c3de95cb9f
Source noteuspto-grants-2016_07