Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249033Generated: October 31, 2026

Sodium borohydride → 4-(5-Phenoxypent-1-ynyl)benzyl alcohol

https://huagongshe.com/reaction/2249033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(5-Phenoxypent-1-ynyl)benzaldehydeHCID 14576780—
SolventEthanolHCID 702—
Product4-(5-Phenoxypent-1-ynyl)benzyl alcoholHCID 14576781101.2%

Reaction Steps

A solution of 2.02 g of 4-(5-phenoxy-1-pentyn-1-yl)benzaldehyde in 5 ml of absolute ethanol was stirred with 0° C. bath cooling and 640 mg of sodium borohydride was added in portions. After stirring for 55 minutes the reaction mixture was quenched by the addition of water and then evaporated in vacuo. The residue was mixed cautiously with 2% sulfuric acid and extracted twice with ethyl acetate. The combined extracts were washed with saturated sodium chloride and then a sodium hydrogen carbonate solution. They were dried over magnesiumsulfate and evaporated in vacuo to yield 2.06 g of the 4-(Phenoxy-1-pentyn-1-yl)-benzyl alcohol which was sufficiently pure to use without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041638
Source datasetuspto-grants-1991_08
ORD IDord-85e440bc213248d590b99b14e97d223f
Source noteuspto-grants-1991_08