Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248542Generated: October 31, 2026

4-tert-Butylphenol → HCID 14743498, compound

https://huagongshe.com/reaction/248542

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 benzyltrimethylammonium 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 numberUS05210234
Source datasetuspto-grants-1993_05
ORD IDord-d46d29c4ec22420787fc590b1cef94d9
Source noteuspto-grants-1993_05