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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490012Generated: November 3, 2026

Epichlorohydrin → HCID 21480268, compound

https://huagongshe.com/reaction/1490012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14346271HCID 14346271—
SolventTolueneHCID 1140—
ProductHCID 21480268HCID 21480268—

Reaction Steps

12.72 g (18.2 mmol) of 2-[4-hydroxybenzyl)-1,4,7,10-tetrakis-(tert-butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (example 9d) is dissolved in 250 ml of toluene and mixed with 350 mg of sodium hydride (80% in paraffin, 18.3 mmol). It is warmed to 80° to 100° C. and mixed by instillation with a solution of 1.74 g (18.2 mmol) of epichlorohydrin in 50 ml of toluene. After refluxing for two hours, it is concentrated by evaporation and purified over a silica gel column. A colorless oil is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681543
Source datasetuspto-grants-1997_10
ORD IDord-ead090d7285c4b35aa99560bcae6b455
Source noteuspto-grants-1997_10