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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258412Generated: October 26, 2026

Benzaldehyde → 4-(5-Phenoxypentyl)benzyl alcohol

https://huagongshe.com/reaction/258412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(5-Phenoxypent-1-ynyl)benzyl alcoholHCID 14576781—
SolventEthanolHCID 702—
SolventSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
Product4-(5-Phenoxypentyl)benzyl alcoholHCID 1457678299%

Reaction Steps

4-(5-Phenoxypent-1-ynyl)benzyl alcohol--To a solution of 2.02 g of 4-5-phenoxypent-1-ynyl)benzaldehyde (from step (2) above) in 50 mL ethanol at 0° C. was added 640 mg sodium borohydride. After stirring for 1 hour, then addition of 8 mL water and evaporation of the solvents in vacuo, the residue was diluted with 2% H2SO4 and ethyl acetate. The organic layer was washed with brine and saturated NaHCO3 and then dried and the solvent evaporated in vacuo to give the title compound (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266713
Source datasetuspto-grants-1993_11
ORD IDord-3025a1c049d14277abbf116508c1d341
Source noteuspto-grants-1993_11