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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487898Generated: October 30, 2026

trans-2,3-Dimethyloxirane → 2,6-Bis(1,1-dimethylethyl)-4-[(2-hydroxy-1-methylpropyl)thio]phenol

https://huagongshe.com/reaction/487898

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-2,3-DimethyloxiraneHCID 30664—
Reactant2,6-Di-tert-butyl-4-mercaptophenolHCID 70370—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Product2,6-Bis(1,1-dimethylethyl)-4-[(2-hydroxy-1-methylpropyl)thio]phenolHCID 14011812—

Reaction Conditions

Temperature5 °C

Reaction Steps

2,6-bis(1,1-Dimethylethyl)-4-mercaptophenol (18.2 g, 0.076 mole) was added to a solution of sodium ethoxide freshly prepared from sodium (3.5 g, 0.15 mole) in ethyl alcohol (100 ml) and stirred for 1 hour. After cooling to 5° C. with an ice bath, trans-2,3-epoxybutane (5.0 g, 0.069 mole) was added and the ice bath removed. After stirring for 5.5 hours the reaction mixture was poured into ten percent hydrochloric acid (50 ml). The ethyl alcohol was removed using a rotary evaporator and the aqueous residue extracted with ethyl acetate (2×75 ml). The extracts were combined, dried over sodium sulfate, filtered, and concentrated to an orange oil. The product was purified by chromatography on silica to give a yellow solid which was recrystallized from hexane to give a white solid, m.p. ca. 73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298514
Source datasetuspto-grants-1994_03
ORD IDord-bb63a57b327248f48899910fcc1735ee
Source noteuspto-grants-1994_03