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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72423Generated: October 25, 2026

1-Chloroethyl chloroformate → 3-(4-Fluorophenoxy)azetidine

https://huagongshe.com/reaction/72423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant1-Benzhydryl-3-(4-fluorophenoxy)azetidineHCID 15053369—
Solvent1,2-DichloroethaneHCID 11—
Product3-(4-Fluorophenoxy)azetidineHCID 2142873099.9%

Reaction Steps

1-chloroethyl chloroformate (0.87 ml, 8.09 mmol) was added to an ice-cooled solution of 1-benzhydryl-3-(4-fluorophenoxy)azetidine (D21) (1.8 g, 5.39 mmol) in 1,2 dichloroethane (18 ml) and the resulting mixture was heated under reflux for 3 hours. The reaction mixture was evaporated in vacuo and the residue was re-dissolved in methanol (10 ml). This solution was heated under reflux overnight then cooled at room temperature and evaporated in vacuo. The obtained residue was loaded on SPE-SCX (20 g) cartridge. The ammonia fractions, after evaporation in vacuo, were loaded on by SPE-Si (5 g) cartridge eluting with a mixture dichloromethane/dichloromethane:NH3 (2M solution in MeOH) (from 100/0 to 80/20). Collected fractions after solvent evaporation afforded the title compound (D49) (0.9 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828987B2
Source datasetuspto-grants-2014_09
ORD IDord-c055887e6a81427db20809de6ebda7cf
Source noteuspto-grants-2014_09