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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597647Generated: November 1, 2026

Sodium ethoxide → HCID 54527180, compound

https://huagongshe.com/reaction/597647

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 numberUS04014920
Source datasetuspto-grants-1977_03
ORD IDord-5b47a30df0e0463e8601d908742d0e04
Source noteuspto-grants-1977_03