Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504296Generated: October 31, 2026

Tert-butyl 3-(trichloromethyl)oxaziridine-2-carboxylate → Tert-butyl 2-(3-benzylpentan-3-yl)hydrazinecarboxylate

https://huagongshe.com/reaction/1504296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(trichloromethyl)oxaziridine-2-carboxylateHCID 11139943—
Reactant3-Benzylpentan-3-amineHCID 18506351—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 2-(3-benzylpentan-3-yl)hydrazinecarboxylateHCID 89807785—

Reaction Steps

2.68 g of 3-benzylpentan-3-amine was dissolved in 20 mL of methylene chloride, mixed with 4.8 g (18 mmol) of separately prepared t-butyl 3-(trichloromethyl)-1,2-oxaziridine-2-carboxylate under cooling with ice, and stirred at room temperature for 30 minutes, and the reaction solution was washed with 10% aqueous citric acid, with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively and dried over anhydrous sodium sulfate, and methylene chloride was removed under reduced pressure. The resulting residue was purified by intermediate pressure silica gel column chromatography (silica gel 30 g, ethyl acetate:hexane=0:100 to 20:80) to give 1.62 g of the desired product as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212348B2
Source datasetuspto-grants-2015_12
ORD IDord-4a4f4af356664bd4a8a462fb3f696386
Source noteuspto-grants-2015_12