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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109844Generated: October 30, 2026

2-[(Benzyloxy)methyl]-1-tritylaziridine → 2-[(Benzyloxy)methyl]aziridine

https://huagongshe.com/reaction/2109844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(Benzyloxy)methyl]-1-tritylaziridineHCID 78156232—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
SolventTriethylsilaneHCID 12052—
Product2-[(Benzyloxy)methyl]aziridineHCID 86602786—

Reaction Steps

To a cold (0° C.) solution of 2-[(benzyloxy)methyl]-1-tritylaziridine (1.28 g, 3.16 mmol) in dichloromethane (13 mL), trifluoroacetic acid (1 mL) and triethylsilane (2.0 mL) was added and stirred at the temperature for 1 h. The resultant mixture was concentrated under vacuum, and the residue was partitioned between ether and brine. The organic extract was dried with anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with a mixture of 50-100% THF in hexane. Collection and concentration of appropriate fractions provided 2-[(benzyloxy)methyl]aziridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-22c1b535cf6d413b91a75cd5230e7cd9
Source noteuspto-grants-2009_04