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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765815Generated: October 25, 2026

Sodium borohydride → 5-(tert-Butyl)-2-(hydroxymethyl)phenol

https://huagongshe.com/reaction/1765815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-tert-Butyl-2-hydroxybenzaldehydeHCID 13765272—
ReactantTrifluoro-methanesulfonic acid 5-tert-butyl-2-formyl-phenyl esterHCID 57424249—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-(tert-Butyl)-2-(hydroxymethyl)phenolHCID 19690241—

Reaction Steps

A stirred, cooled (ice-bath) solution of a 1:1 mixture of trifluoro-methanesulfonic acid 5-tert-butyl-2-formyl-phenyl ester and 4-tert-butyl-2-hydroxy-benzaldehyde (Intermediate 105, 0.47 g) in methanol (8 mL) was treated with sodium borohydride (0.1 g, 2.64 mmol). After 1 h, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to a residue that was subjected to flash column chromatography on silica gel (230–400 mesh) to afford the title product (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226951B2
Source datasetuspto-grants-2007_06
ORD IDord-b69e4c0de991430db3f0d33b68181095
Source noteuspto-grants-2007_06