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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557857Generated: November 1, 2026

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

https://huagongshe.com/reaction/557857

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 numberUS08058288B2
Source datasetuspto-grants-2011_11
ORD IDord-250de9df8d3545d59d6186c5fe27e56a
Source noteuspto-grants-2011_11