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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597641Generated: October 30, 2026

Sodium Methoxide → HCID 54559983, compound

https://huagongshe.com/reaction/597641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 53654074HCID 53654074—
SolventMethanolHCID 887—
ProductHCID 54559983HCID 54559983—

Reaction Conditions

Temperature50 °C

Reaction Steps

13.0 g (0.05 mol) of p-(2-acetylaminovinyl)-acetoxy-benzene are suspended in 100 ml of absolute methanol, a solution of 2.8 g (0.05 mol) of sodium methoxide in 20 ml of absolute methanol is added and thereafter the mixture is warmed to 50°C for 15 minutes. It is then evaporated to dryness in vacuo. The resulting crude phenolate of p-(2-acetylaminovinyl)-phenol is heated with 65 ml of epichlorohydrin to the boil for 18 hours, under a reflux condenser and whilst stirring. Thereafter, the excess epichlorohydrin is removed by vacuum distillation. The residue is partitioned between water and ethyl acetate and the organic phase is siphoned off, dried over sodium sulphate and evaporated. After crystallisation of the crude product, thus obtained, from acetone-ether, 1-[p-(2-acetylaminovinyl)-phenoxy]-2,3-epoxy-propane of melting point 135°-137°C is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014920
Source datasetuspto-grants-1977_03
ORD IDord-b883c6afa5734989960945c16172cc05
Source noteuspto-grants-1977_03