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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantTetrahydrofuranHCID 8028—
ReactantN-(4-Methoxyphenyl)-2,2-dimethylpropanamideHCID 521748—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductN-[2-(2-Hydroxyethyl)-3-methoxyphenyl]-2,2-dimethylpropanamideHCID 1266969769%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04287201
Source datasetuspto-grants-1981_09
ORD IDord-5dd1f8aa5149401a90f906e6d21522dd
Source noteuspto-grants-1981_09