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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073756Generated: October 31, 2026

3-Cyclopentyloxy-4-methoxybenzaldehyde → 3-Cyclopentyloxy-4-methoxybenzyl alcohol

https://huagongshe.com/reaction/1073756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product3-Cyclopentyloxy-4-methoxybenzyl alcoholHCID 11138706—

Reaction Steps

To a stirred solution of 10.42 g (47.3 mmol) of 3-cyclopentoxy-4-methoxybenzaldehyde in 100 mL of absolute ethanol was added 0.9 g (23.8 mmol) of sodium borohydride in one portion. The mixture was stirred for 1 hour at room temperature after which time the reaction was quenched with excess acetic acid, concentrated and azeotroped to dryness three times with 25 mL portions of toluene. The residue was dissolved in 100 mL of chloroform, washed with two, 25 mL portions of saturated sodium chloride, dried over magnesium sulfate, and concentrated to dryness. Liquid chromatography of the crude oil over 200 g of silica gel with 10% ethyl acetate in hexane provided an analytically pure oil after drying in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971959
Source datasetuspto-grants-1990_11
ORD IDord-15b7078276274595963a7dd4c41ae85b
Source noteuspto-grants-1990_11