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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275574Generated: October 31, 2026

Benzyl Alcohol → 1-[6-(Benzyloxy)pyridin-3-yl]cyclopropanecarboxylic acid

https://huagongshe.com/reaction/2275574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 1-(6-chloropyridin-3-yl)cyclopropanecarboxylateHCID 86602273—
SolventEthyl AcetateHCID 8857—
Product1-[6-(Benzyloxy)pyridin-3-yl]cyclopropanecarboxylic acidHCID 66661660—

Reaction Steps

A mixture of ethyl 1-(6-chloropyridin-3-yl)cyclopropanecarboxylate (45.1 mg, 0.000200 mol), benzyl alcohol (0.50 mL, 0.0048 mol) and sodium hydride (9.50 mg, 0.000238 mol) was irradiated by microwave at 150° C. for 15 minutes. After cooling, additional sodium hydride (9.5 mg) was added to the mixture. The mixture then was irradiated by microwave at 150° C. for 15 minutes. Ethyl acetate (5 mL) was added and the resulting mixture was washed with water and brine successively. The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by Combiflash with ethyl acetate/hexane to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126927B2
Source datasetuspto-grants-2015_09
ORD IDord-8c920161069f461c986a2786460e9f05
Source noteuspto-grants-2015_09