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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660547Generated: October 31, 2026

Sodium borohydride → 3-Benzyloxy-4-nitro-benzyl alcohol

https://huagongshe.com/reaction/660547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(Benzyloxy)-4-nitrobenzaldehydeHCID 12111719—
SolventMethanolHCID 887—
Product3-Benzyloxy-4-nitro-benzyl alcoholHCID 54518781—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Benzyloxy-4-nitrobenzaldehyde (10.3 g, 0.040 mol) is dissolved in methanol (120 mL) with heating and then cooled to 0° C. To this stirred solution, sodium borohydride (1.5 g, 0.40 mol) is added in portions over a period of 5 min. The mixture is allowed to warm to RT and stirred for 18 h. The solvent is removed under reduced pressure and EtOAc is added. The organic layer is washed with 1N HCl and brine, dried over sodium sulfate/magnesium sulfate, and concentrated to afford the title compound as a yellow-brown solid: (M+NH4)+=277.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-11676f4489a841f4ba7893945e808882
Source noteuspto-grants-2011_12