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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461532Generated: November 1, 2026

4-tert-Butylphenol → HCID 14743498, compound

https://huagongshe.com/reaction/1461532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14743498HCID 14743498—

Reaction Steps

4-t-butylphenol (10 g) and sodium hydroxide (3.99 g) were added to a stirred mixture of water (60 ml) and dichloromethane (60 ml) followed by benzyltrimethyl-ammonium hydroxide (40% solution in methanol, 150 ml) and 3-chloro-3-methyl-butyne (13.65 g). After stirring at ambient temperature for 11 days, the layers were separated and the aqueous layer extracted with chloroform. The combined organic extracts were concentrated in vacuo and the residue dissolved in diethyl ether. The solution was washed with water, 10% sodium hydroxide solution, then brine, and dried over magnesium sulphate. Removal of drying agent and solvent gave 3-methyl-3-(4-t-butylphenoxy)-but-1-yne as a yellow oil (13.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075460
Source datasetuspto-grants-1991_12
ORD IDord-4a9103a9fb2144f88efeb4d51923d475
Source noteuspto-grants-1991_12