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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276455Generated: October 31, 2026

Benzyl chloroformate → 3-(N-Carbobenzyloxy-3-fluoroanilin-4-yl)-3-hydroxy-1-(1,1-diphenylmethyl)azetidine

https://huagongshe.com/reaction/1276455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(4-Amino-2-fluorophenyl)-3-hydroxy-1-(1,1-diphenylmethyl)azetidineHCID 22625705—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-(N-Carbobenzyloxy-3-fluoroanilin-4-yl)-3-hydroxy-1-(1,1-diphenylmethyl)azetidineHCID 22625675—

Reaction Steps

To a solution of 3-(4-amino-2-fluorophenyl)-3-hydroxy-1-(1,1-diphenylmethyl)azetidine (Example 81, Step 1, 5.10 g, 14.7 mmol) in acetone (75 mL) was added a solution of sodium bicarbonate (2.52 g, 30.0 mmol) in water (40 mL) to give a creamy suspension. Benzyl chloroformate (2.57 g, 15.1 mmol) was added and stirring continued overnight. The suspension was filtered and the acetone evaporated. The residue was partitioned between ethyl acetate (200 mL) and water (50 mL). The organic layer was washed with brine (50 mL), dried over magnesium sulfate, filtered and evaporated to leave an amber foam. Chromatography over silica gel (150 g, 40-60 μM) eluting with 1-2% methanol-methylene chloride gave the title compound as a cream foam. HRMS: meas. 483.2087, theory 483.2084.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166056
Source datasetuspto-grants-2000_12
ORD IDord-e77414a63ae64e289e6e7a0b2fdff898
Source noteuspto-grants-2000_12