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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414250Generated: October 30, 2026

Benzyl Alcohol → 2-(benzyloxy)-6-chloropyrazine

https://huagongshe.com/reaction/414250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2,6-DichloropyrazineHCID 78504—
SolventBenzeneHCID 241—
Product2-(benzyloxy)-6-chloropyrazineHCID 1174616586.5%

Reaction Steps

7.6 g of benzylalcohol was dissolved in 65 ml of benzene, and 2.8 g of 60% sodium hydride was added little by little to the solution under stirring not so as to foam too much at room temperature. After the addition, stirring was continued for 10 min. at room temperature, followed by reflux for 1 hour. Subsequently, the solution was cooled to 50° to 60° C., and added dropwise with a solution of 10 g of 2,6-dichloropyrazine in 65 ml of benzene for 10 min. Then, after reflux for 4 hours, the reaction was finished. After cooling below 10° C., about 100 ml of water was added, and the separated benzene layer was collected. The residue obtained by distilling off the solvent was purified by silica-gel column chromatography (developing solvent: n-hexane and ethyl acetate) to obtain 12.8 g of 2-benzyloxy-6-chloropyrazine as a colourless oil (yield: 86.5%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791127
Source datasetuspto-grants-1988_12
ORD IDord-0d078e38300142b0a8e429f46b8b848d
Source noteuspto-grants-1988_12