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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634016Generated: October 25, 2026

Water → 1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-ol

https://huagongshe.com/reaction/634016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Bromo-1-benzofuranHCID 640589—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-olHCID 67154652—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2.5 M solution of n-butyllithium in hexanes (2.23 mL, 5.58 mmol) was added dropwise to a solution of 3-bromobenzofuran (1.0 g, 5.08 mmol) in THF (35 mL) at −78° C. The reaction mixture was stirred for 30 minutes at −78° C. and then a solution of 1-benzhydrylazetidin-3-one (1.2 g, 5.08 mmol, as prepared in step 1 of example FAB270) in THF (10 mL) was added dropwise at the same temperature. The mixture was allowed to warm back to room temperature overnight. Water (50 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel using petroleum ether/dichloromethane (50:50 to 0:100) as eluent. The title compound was obtained as a yellow solid (230 mg, 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321769B2
Source datasetuspto-grants-2016_04
ORD IDord-8bda8f9d55ac4d60b951a945dda3155c
Source noteuspto-grants-2016_04