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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403114Generated: October 30, 2026

(2-Tert-butoxyphenyl)methanol → 2-tert-Butoxybenzaldehyde

https://huagongshe.com/reaction/403114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Tert-butoxyphenyl)methanolHCID 21060300—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product2-tert-ButoxybenzaldehydeHCID 1495552670%

Reaction Steps

To a stirred solution of 7 (3.8 g, 21 mmol) in 250 mL CH2Cl2, MnO2 (11 g, 126 mmol) was added. The reaction mixture was stirred overnight, filtered on Celite® and the solvent was distilled under reduced pressure. The crude product was purified by a silica gel column with 17% EtOAc/83% Hexane as eluents. The product was isolated as pale yellow oil (70% yield). 1H NMR (CDCl3) δ 7.286 (dd, 1H, Ar), 7.195 (ddd, 1H, Ar), 7.063 (d, 1H, Ar), 7.003 (ddd, 1H, Ar), 4.669 (s, 2H, —CH2—), 1.447 (s, 9H, —C(CH3)3). Mass Spec.=203.09 (M+H)++Na+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08747810B2
Source datasetuspto-grants-2014_06
ORD IDord-132e8456c18a42d5a308eec9eb6c660a
Source noteuspto-grants-2014_06