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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425382Generated: November 3, 2026

Benzhydrylamine → trans(+/-)-1-(Diphenylmethyl)-2-ethylazetidin-3-ol

https://huagongshe.com/reaction/1425382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylamineHCID 7036—
ReactantHCID 86648813HCID 86648813—
SolventMethanolHCID 887—
Producttrans(+/-)-1-(Diphenylmethyl)-2-ethylazetidin-3-olHCID 8664881248.6%

Reaction Steps

Benzhydrylamine (1.04 mL, 6.06 mmol) was added to a solution of (2R*)-2-[(1R*)-1-bromopropyl]oxirane obtained in Example (234a) (1.00 g, 6.06 mmol) in methanol (6 mL), and the mixture was heated under reflux for 17 hours. The reaction solution was concentrated under reduced pressure. Saturated aqueous sodium carbonate solution was added to the resulting residue, followed by extraction with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate. Following filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=2/1) to obtain 787 mg of the title compound as a colorless oily substance (49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-2b4925af887e46c0ad3b066a097ee00e
Source noteuspto-grants-2015_01