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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417729Generated: November 4, 2026

2-tert-Butyl-4-hydroxyanisole → 2-tert-Butyl-4-hydroxyanisole

https://huagongshe.com/reaction/2417729

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-4-hydroxyanisoleHCID 6932—
ReactantTert-ButylhydroquinoneHCID 16043—
SolventMethanolHCID 887—
Product2-tert-Butyl-4-hydroxyanisoleHCID 6932—
ProductButylated HydroxyanisoleHCID 8456—

Reaction Steps

5.0 g of tert-butyl-hydroquinone, 40 cm3 of methanol and 1.0 g of cupric chloride are fed into the autoclave. The autoclave is purged with nitrogen and kept at 105° C. for 2.5 hours. On termination of the reaction, mixture analysis indicates the formation of 4.4 g of tert-butyl-hydroquinone monomethyl ether (BHA) (conversion 100%, selectivity 82%). The two BHA isomers (3-tert-butyl-4-hydroxyanisole and 2-tert-butyl-4-hydroxyanisole) are formed in a weight ratio of 99:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469897
Source datasetuspto-grants-1984_09
ORD IDord-0a1acd4bef8c441bb685e10cda75f930
Source noteuspto-grants-1984_09