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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473337Generated: October 31, 2026

1-(Diphenylmethyl)azetidin-3-ol → 1-(Diphenylmethyl)azetidin-3-one

https://huagongshe.com/reaction/1473337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Diphenylmethyl)azetidin-3-olHCID 330448—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—

Reaction Conditions

Temperature50 °C

Reaction Steps

The title compound was prepared as described in WO2010079443A1. To a solution of compound 1-benzhydrylazetidin-3-ol (20 g, 28.4 mmol) in the triethyl amine (60 mL) was added a solution of sulfur trioxide pyridine complex (SO3.Py) (40 g, 251.6 mmol) in dimethylsulfoxide (260 mL) under a nitrogen atmosphere at 25° C. The reaction was stirred at 50° C. for 2 h. Then the reaction mixture was cooled back to 25° C., diluted with water (500 mL), and extracted with ethyl acetate (2×500 mL). Organic part was dried over sodium sulfate, filtered, and concentrated under a vacuum to give a crude compound which was further purified by column chromatography using silica gel (100 to 200 mesh) eluting with 0% to 20% ethyl acetate in hexanes to provide 1-benzhydrylazetidin-3-one (11.7 g) as a white solid. MS (ESI, positive ion) m/z (M+1): 238.30. 1H NMR (400 MHz, DMSO) δ 7.50 (d, J=7.5 Hz, 4H), 7.30 (t, J=7.5 Hz, 4H), 7.20 (t, J=7.3 Hz, 2H), 4.82 (s, 1H), 4.00 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-91d1743e54494d7ea727238ee7bb9c4d
Source noteuspto-grants-2015_04