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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657347Generated: October 29, 2026

3-Bromobenzaldehyde → 3-Bromobenzyl alcohol

https://huagongshe.com/reaction/657347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product3-Bromobenzyl alcoholHCID 8514199.8%

Reaction Steps

Sodium borohydride (7.1 g, 186.1 mmol) in several portions was added to a solution of 3-bromobenzaldehyde (114.8 g, 620.4 mmol) in EtOH (650 mL) at 25° C. Then the mixture was stirred for 1 h at room temperature. The reaction was quenched with water (200 mL). After removing EtOH, the residue was dissolved in AcOEt (500 mL), and filtered. The filtrate was washed with water (150 mL), brine (150 mL), and dried over Na2SO4. After removing the solvent, 115.8 g of the title compound was obtained (yield: 99.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071588B2
Source datasetuspto-grants-2011_12
ORD IDord-a6df00b9960a408aacde8fbedd51f757
Source noteuspto-grants-2011_12