HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577152Generated: November 2, 2026
Ethylene Oxide → N-[2-(2-Hydroxyethyl)-3-methoxyphenyl]-2,2-dimethylpropanamide
https://huagongshe.com/reaction/1577152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-(4-Methoxyphenyl)-2,2-dimethylpropanamide | HCID 521748 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-[2-(2-Hydroxyethyl)-3-methoxyphenyl]-2,2-dimethylpropanamide | HCID 12669697 | 69% |
Reaction Steps
To N-pivaloylanisidine (4.14 g, 0.02 mole) in freshly distilled THF (60 ml) under nitrogen is added 2.3 N butyllithium in hexane (23 ml) at 0° C. and the resultant solution is stirred at 0° C. for 2 hours. Ethylene oxide (liquid, 1.6 ml) is added and the reaction mixture is stirred for an hour at 0° C. and then an additional hour at ambient temperature. Acetic acid (2 ml) and water (30 ml) are added to quench the reaction. The THF is evaporated in vacuo and the aqueous mixture is extracted with ether (2×30 ml). The extracts are combined, washed with 5% sodium bicarbonate solution, brine, dried over sodium sulfate and concentrated to 5.42 g of crystalline material. Recrystallization from n-butyl chloride (13 ml) gives 3.46 g (69%) of 2-(2-hydroxyethyl)-3-pivalamidoanisole, m.p. 118°-119.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04287201 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-5dd1f8aa5149401a90f906e6d21522dd |
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| Source note | uspto-grants-1981_09 |
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