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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845083Generated: October 29, 2026

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

https://huagongshe.com/reaction/845083

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 numberUS04755524
Source datasetuspto-grants-1988_07
ORD IDord-8feea872517749a49a131a8a4ed733b2
Source noteuspto-grants-1988_07