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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979667Generated: October 30, 2026

Epichlorohydrin → HCID 13371497, compound

https://huagongshe.com/reaction/979667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantHCID 13371496HCID 13371496—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventWaterHCID 962—
ProductHCID 13371497HCID 13371497—

Reaction Conditions

Temperature110 °C

Reaction Steps

In a flask, the mixture of 35 g of 2-carbethoxy 4-(5-methyl-2-thiophene carboxamido)phenol and 175 ml of epichlorohydrin, is heated to 110° C., then 2.9 g of benzyltrimethylammonium chloride are introduced. The reaction mixture is then heated to reflux for 30 mins., then cooled. Once the temperature of the medium has dropped again to 50° C., 200 ml of water are added and the mixture is stirred strongly. After decantation, the aqueous phase is extracted twice with ether and the organic phases are dried over magnesium sulfate, filtered and concentrated in vacuo. The residue hardens in ether. After three washings in 50 ml of isopropylic ether, 30 g of 1-[2-carbethoxy 4-(5-methyl 2-thiophene carboxamido)phenoxy]2,3-epoxy propane are obtained in the form of white crystals melting at 109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668801
Source datasetuspto-grants-1987_05
ORD IDord-0368a86019174ec9a71068aa1c545ff5
Source noteuspto-grants-1987_05