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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463108Generated: November 2, 2026

Epichlorohydrin → HCID 20135273, compound

https://huagongshe.com/reaction/1463108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactant2-MethoxyethanolHCID 8019—
ReactantSodium HydroxideHCID 14798—
ReactantPhenol, 4,4'-(1-methylethylidene)bis(2-(2-propen-1-yl)-HCID 74457—
ProductHCID 20135273HCID 20135273604.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

2,2-Bis(3-allyl-4-hydroxyphenyl)propane (308 g) was mixed with 2-methoxyethanol (10 g) and epichlorohydrin (740 g) and heated to 60° C. Sodium hydroxide flake (80 g) was added portionwise over 3 hours, and the mixture was stirred for a further 1/2 hour, also at 60° C. The mixture was filtered, the residue being washed with toluene, and the filtrate was evaporated to remove the solvents and the excess of epichlorohydrin. The concentrated product was filtered once more to give 334 g of 2,2-bis(3-allyl-4-(glycidyloxy)phenyl)propane, having an epoxide content of 4.03 equiv./kg and 4.5 allyl double bond equiv./kg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04463169
Source datasetuspto-grants-1984_07
ORD IDord-f7f184fc8c6648b4b89b8457daf474b7
Source noteuspto-grants-1984_07