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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633558Generated: October 30, 2026

Tetrahydrofuran → Cyclopropyl-(3-methoxyphenyl)-(3-pyridinyl)methanol

https://huagongshe.com/reaction/1633558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(3-Methoxybenzoyl)pyridineHCID 10036137—
ProductCyclopropyl-(3-methoxyphenyl)-(3-pyridinyl)methanolHCID 15552043—

Reaction Steps

To a solution of (3-methoxyphenyl)-(3-pyridinyl)methanone (500 mg) in THF (10 ml) was added 1.1M cyclopropylmagnesium bromide THF solution (2 ml) at 0° C. The reaction mixture was warmed to room temperature, and stirred for 30 minutes. Aqueous ammonium chloride and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was filtered and washed with ethyl acetate-hexane (1:2) to give cyclopropyl-(3-methoxyphenyl)-(3-pyridinyl)methanol (470 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503926B2
Source datasetuspto-grants-2003_01
ORD IDord-cc63e8ec1ea0433c872301910b1cc01e
Source noteuspto-grants-2003_01