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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721413Generated: October 30, 2026

1,4-Butanediol → 4-(3-Tert-butyl-5-methyl-4-hydroxyphenyl)butanol

https://huagongshe.com/reaction/1721413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-ButanediolHCID 8064—
ReactantPotassium HydroxideHCID 14797—
Reactant2-tert-Butyl-6-methylphenolHCID 16678—
Product4-(3-Tert-butyl-5-methyl-4-hydroxyphenyl)butanolHCID 21199344—

Reaction Conditions

Temperature235 °C

Reaction Steps

50 g of potassium hydroxide, 316 g of 2-tert-butyl-6-methylphenol and 866 g of 1,4-butanediol are initially introduced into an autoclave. After introducing nitrogen gas, the autoclave is closed and the mixture is heated at 235° C. (4 bar) for 6 hours, with stirring; a further rise in pressure as a consequence of the reaction is prevented by blowing of gas. When the reaction is complete, the reaction mixture is cooled to 80° C. and the autoclave is emptied. Excess butanediol is removed by distillation. The distillation residue is poured into 11 of water and 500 ml of toluene. The organic phase is then washed with water until neutral and the toluene is stripped off by applying a vacuum. The remaining residue (310 g) contains 68-70% of the title product of the formula ##STR25##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510402
Source datasetuspto-grants-1996_04
ORD IDord-0c75f0beb66a47fda5b373700f6c334a
Source noteuspto-grants-1996_04