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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052787Generated: October 30, 2026

2-Chloro-4-t-butylbenzyl alcohol → 4-tert-Butyl-2-chlorobenzaldehyde

https://huagongshe.com/reaction/2052787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-t-butylbenzyl alcoholHCID 68899078—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product4-tert-Butyl-2-chlorobenzaldehydeHCID 1785961079%

Reaction Conditions

Temperature50 °C

Reaction Steps

The alcohol compound (195 mg, 0.981 mmol) obtained in Step 1-3 was dissolved in chloroform (5 ml). Activated manganese dioxide (1.27 g) was added to the obtained solution, and they were violently stirred at 50° C. for 2 hours. After leaving to cool, manganese dioxide was filtered out, and the filtrate was concentrated under reduced pressure. After the purification by the silica gel column chromatography, 2-chloro-4-t-butylbenzaldehyde (yield: 152 mg, 79%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326701B2
Source datasetuspto-grants-2008_02
ORD IDord-27fb604fb5af4837a01fa0452c05b2b7
Source noteuspto-grants-2008_02