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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073232Generated: October 30, 2026

Ethanol → HCID 15027735, compound

https://huagongshe.com/reaction/1073232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant2,6-Di-tert-butyl-4-mercaptophenolHCID 70370—
Reactant2-(Bromomethyl)benzonitrileHCID 89599—
SolventWaterHCID 962—
ProductHCID 15027735HCID 1502773518.9%

Reaction Steps

A solution of 2.00 g (8.39 mmole) of 2,6-di-t-butyl-4-mercaptophenol, 1.65 g (8.39 mmole) of o-cyanobenzyl bromide, 5 ml of 1.68N sodium hydroxide and 75 ml of ethanol was heated at reflux for 48 hours. The reaction mixture was poured into water and was extracted with diethyl ether. The ether extract was washed with water, dried with magnesium sulfate and evaporated to give the crude product as an oil. The oil was purified by silica gel chromatography, eluting with a mixture of ethyl acetate and hexane, followed by recrystallization from hexane to give 0.56 g of white 2,6-di-t-butyl-4-[(2-cyanophenyl) methylthio]phenol, m.p. 79°-82° C. Analysis: Calculated for C22H27NOS: %C, 74.7; %H, 7.7; %N, 4.0; Found: %C, 74.6; %H, 7.9; %N 3.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968710
Source datasetuspto-grants-1990_11
ORD IDord-93227793450949f78125c6a97f67ca1d
Source noteuspto-grants-1990_11