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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346333Generated: October 30, 2026

Sodium borohydride → 5-Benzyloxy-2-methoxybenzyl alcohol

https://huagongshe.com/reaction/346333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(Benzyloxy)-2-methoxybenzaldehydeHCID 10966694—
SolventMethanolHCID 887—
Product5-Benzyloxy-2-methoxybenzyl alcoholHCID 1433313295%

Reaction Steps

5-Benzyloxy-2-methoxybenzaldehyde (150.4 g) was suspended in methanol (600 ml) and to the gently warmed stirred mixture was added, in portions, sodium borohydride (15.0 g). The methanol was evaporated and the residue partitioned between dichloromethane and water. The organic layer was washed with water, then saturated sodium chloride, dried with anhydrous magnesium sulphate and evaporated to dryness. The residue crystallised from dichloromethane/petroleum spirit (40-60°) to give 5-benzyloxy-2-methoxybenzyl alcohol (143.8 g, 95%), m.p. 50-51°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061798
Source datasetuspto-grants-1991_10
ORD IDord-bfe7e8f168404fb7b3a520b6b55b9252
Source noteuspto-grants-1991_10