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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399163Generated: November 2, 2026

o-CRESYL GLYCIDYL ETHER → HCID 21333213, compound

https://huagongshe.com/reaction/2399163

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-CRESYL GLYCIDYL ETHERHCID 16640—
ReactantHCID 21333189HCID 21333189—
SolventIsopropanolHCID 3776—
ProductHCID 21333213HCID 21333213—

Reaction Steps

A solution of 4.92 g of 1-(o-methyl-phenoxy)-2,3-epoxypropane and 4.59 g of 2-methyl-3-(2-amino-ethoxy)pyrazine in 150 ml of isopropanol is stirred for 24 hours at about 20° C. and thereafter a further 1.47 g of 1-(o-methyl-phenoxy)-2,3-epoxy-propane are added. After standing for a further 24 hours at about 20° C., the reaction mixture is evaporated under a waterpump vacuum, the residue is dissolved in ether, the ether solution is extracted by shaking with 2 N hydrochloric acid and the combined hydrochloric acid extracts are rendered alkaline with sodium hydroxide solution and extracted by shaking with ether. The combined ether extracts are washed with water, dried over sodium sulphate and evaporated under a waterpump vacuum. The residue crystallises from methylene chloride/petroleum ether, giving 1-[2-(2-methyl-3-pyrazinyloxy)-ethyl-amino]-3-(2-methyl-phenoxy)-2-propanol; melting point 82°-84° C. The acid fumarate prepared with the calculated amount of fumaric acid crystallises from isopropanol, melting point 140°-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04027027
Source datasetuspto-grants-1977_05
ORD IDord-6ce63723206e4b1c9dfbc701e5d03d9d
Source noteuspto-grants-1977_05