HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742811Generated: October 29, 2026
trans-2,3-Dimethyloxirane → 2,6-Bis(1,1-dimethylethyl)-4-[(2-hydroxy-1-methylpropyl)thio]phenol
https://huagongshe.com/reaction/1742811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | trans-2,3-Dimethyloxirane | HCID 30664 | — |
| Reactant | 2,6-Di-tert-butyl-4-mercaptophenol | HCID 70370 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,6-Bis(1,1-dimethylethyl)-4-[(2-hydroxy-1-methylpropyl)thio]phenol | HCID 14011812 | — |
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 (2X75 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05342838 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-4031cac5629541cab6b49f2a8e5a695d |
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| Source note | uspto-grants-1994_08 |
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