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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172133Generated: October 27, 2026

3-Methylbenzofuran → 1-Benzhydryl-3-(3-methylbenzofuran-2-yl)azetidin-3-ol

https://huagongshe.com/reaction/2172133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbenzofuranHCID 88939—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
SolventTetrahydrofuranHCID 8028—
Product1-Benzhydryl-3-(3-methylbenzofuran-2-yl)azetidin-3-olHCID 6715454931%

Reaction Steps

A solution of 3-methylbenzofuran (550 mg, 4.16 mmol) in dry THF (17 mL) was cooled to −78° C. and LDA (1.8 M in THF/heptane/ethylbenzene) (2.8 mL, 5.04 mmol) was added dropwise under N2 over 5 min. After stirring for 30 min, 1-benzhydrylazetidin-3-one (1.61 g, 6.78 mmol) was added portionwise over 10 min. The reaction was stirred under N2 at −78° C. for 15 min, and was then allowed to warm to rt and stirred for 1.5 h. The reaction was quenched with 0.5N HCl and extracted with EtOAc. The organic layer was washed with water and brine, dried on Na2SO4 and concentrated. The residue was purified by flash chromatography (heptane/EtOAc, 5%→35%), yielding the product (472 mg, 31%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051321B2
Source datasetuspto-grants-2015_06
ORD IDord-aa6bdd44597b452f85bce8c2821f43c6
Source noteuspto-grants-2015_06