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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259604Generated: October 28, 2026

Sodium ethoxide → HCID 54527180, compound

https://huagongshe.com/reaction/259604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 53758998HCID 53758998—
SolventEthanolHCID 702—
ProductHCID 54527180HCID 54527180—

Reaction Conditions

Temperature50 °C

Reaction Steps

5.0 g (0.02 mol) of p-(2-ethoxycarbonylaminovinyl)-acetoxybenzene, after dissolving in 75 ml of absolute ethanol, addition of a solution of 1.36 g (0.02 mol) of sodium ethoxide in 10 ml of absolute ethanol, 15 minutes' heating to 50° C. and subsequent evaporation to dryness in vacuo, yield the crude sodium salt of p-(2-ethoxycarbonylaminovinyl)-phenol. This is heated with 20 ml of epichlorohydrin to the boil for 24 hours under a reflux condenser and whilst stirring. Thereafter, the excess epichlorohydrin is removed by vacuum distillation. The residue is partitioned between water and methylene chloride and the organic phase is separated off, dried over sodium sulphate and evaporated. 1-[p-(2-Ethoxycarbonylaminovinyl)-phenoxy]-2,3-epoxy-propane of melting point 112° -113° C. (from ether) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038414
Source datasetuspto-grants-1977_07
ORD IDord-2fe96e3dfdef4a1da0384cdfb7eb56f4
Source noteuspto-grants-1977_07