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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761618Generated: November 1, 2026

Sodium borohydride → 5-Benzyloxy-2-methoxybenzyl alcohol

https://huagongshe.com/reaction/1761618

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 reidue 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 numberUS04826876
Source datasetuspto-grants-1989_05
ORD IDord-306df501fcb4460e97a83c5d4237d650
Source noteuspto-grants-1989_05