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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415402Generated: October 31, 2026

Ethanol → Teniloxazine

https://huagongshe.com/reaction/1415402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantAminoethyl sulfateHCID 70223—
Reactant2-({2-[(Thiophen-2-yl)methyl]phenoxy}methyl)oxiraneHCID 13277415—
SolventWaterHCID 962—
ProductTeniloxazineHCID 6438129—

Reaction Steps

A mixture of 19 g of 1-[2-(2-thenyl)phenoxy]-2,3-epoxypropane, 65 g of 2-aminoethyl hydrogen sulfate, 40 g of sodium hydroxide, 350 ml of ethanol and 200 ml of water was heated under reflux with stirring for 23 hours. Most of the ethanol was distilled off, and the residue was extracted with two 400 ml portions of ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. To the residue was added a solution of maleic acid in ethanol. The precipitated crystals were purified in the same manner as in Example 1 to give 2-[2-(2-thenyl)phenoxymethyl]morpholine maleate as colorless crystals, melting at 155°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005084
Source datasetuspto-grants-1977_01
ORD IDord-9c3b7e4649d3476ca24bd96d8b593411
Source noteuspto-grants-1977_01