Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073231Generated: October 31, 2026

Ethanol → HCID 15027733, compound

https://huagongshe.com/reaction/1073231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant2,6-Di-tert-butyl-4-mercaptophenolHCID 70370—
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
SolventWaterHCID 962—
ProductHCID 15027733HCID 1502773325.3%

Reaction Steps

A solution containing 2.00g (8.39 mmole) of 2,6-di-t-butyl-4-mercaptophenol, 1.65 g (8.39 mmole) of m-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 then extracted with diethyl ether. The ether extract was washed with water, dried with magnesium sulfate and evaporated to give the crude product. This material was purified by silica gel chromatography eluting with 1% ethyl acetate in hexane, followed by four recrystallizations from hexane to give 0.75g of 2,6-di-t-butyl-4-[(3-cyanophenyl)methylthio]phenol as white needles, m.p. 61°-63° C. Analysis: Calculated for C22H27NOS: %C, 74.7%; %H, 7.7; %N, 4.0; Found: %C. 74.5; %H, 8.0; %N, 3.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968710
Source datasetuspto-grants-1990_11
ORD IDord-c2356ad02f4444d6aa1b5dc582842c2d
Source noteuspto-grants-1990_11