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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359739Generated: October 28, 2026

Isobutylene oxide → HCID 20133513, compound

https://huagongshe.com/reaction/359739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylene oxideHCID 11208—
Reactant2,6-Di-tert-butyl-4-mercaptophenolHCID 70370—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 20133513HCID 20133513—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of sodium ethoxide, freshly prepared from sodium (1.31 g, 57.2 mmole) in ethyl alcohol (200 ml), was added 2,6-bis(1,1-dimethylethyl)-4-mercaptophenol (6.8 g, 28.6 mmole) and the mixture was stirred for one hour. After cooling to 5° C. with an ice bath, 1,1-dimethylethylene oxide (2.06 g, 28.6 mmole) was added and the ice bath removed. After stirring for 5.5 hours the reaction mixture was poured into 10% hydrochloric acid. The ethyl alcohol was removed in vacuo and the aqueous residue was extracted with ethyl acetate. The extracts were combined, dried over sodium sulfate, filtered, and concentrated to give 2,6-bis (1,1-dimethylethyl)-4-[(2-hydroxy-2-methylpropyl)thio]phenol. Trifluoroacetic acid (3 ml) was added to a solution of the phenol intermediate (2.2 g, 7 mmole), followed by addition by syringe of methyl thioglycolate (0.7 g, 6.7 mmole). After three hours the mixture was poured into water (100 ml) and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to an oil. Chromatography on silica gel gave the title dithio compound, m.p. 64°-68°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002967
Source datasetuspto-grants-1991_03
ORD IDord-4b39357762cb466a828cf83cad298811
Source noteuspto-grants-1991_03