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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279651Generated: November 2, 2026

Toluene → 1-Benzyl-4-[3-(tert-butoxycarbonylamino)-1-fluorocyclobutan-3-yl]-2-pyrrolidone

https://huagongshe.com/reaction/1279651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Benzyl-4-[3-(tert-butoxycarbonylamino)-1-hydroxycyclobutan-3-yl]-2-pyrrolidoneHCID 18427824—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-4-[3-(tert-butoxycarbonylamino)-1-fluorocyclobutan-3-yl]-2-pyrrolidoneHCID 1842780030%

Reaction Steps

A 1.79 g (4.96 mmol) portion of 1-benzyl-4-[3-(tert-butoxycarbonylamino)-1-hydroxycyclobutan-3-yl]-2-pyrrolidone (Isomer B1) was dissolved in a mixed solvent consisting of 50 ml of toluene and 20 ml of dichloromethane to which, while cooling in an ice bath with stirring, was then added 1.31 ml (9.92 mmol) of diethylaminosulfur trifluoride, subsequently carrying out 12 hours of stirring at room temperature. While cooling in an ice bath with stirring, the reaction solution was alkalified by slowly adding saturated sodium bicarbonate aqueous solution and then mixed with chloroform to carry out separation of layers, and the resulting organic layer was washed with saturated brine. The aqueous layer was again extracted with chloroform, and the organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under a reduced pressure and the resulting residue was purified by a silica gel column chromatography to give 541 mg (30.0%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448266B1
Source datasetuspto-grants-2002_09
ORD IDord-134ab0e49ef24bd9b17c42f88ff872dc
Source noteuspto-grants-2002_09