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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415403Generated: October 31, 2026

Ethanol → Teniloxazine

https://huagongshe.com/reaction/1415403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantAminoethyl sulfateHCID 70223—
Reactant2-({2-[(Thiophen-2-yl)methyl]phenoxy}methyl)oxiraneHCID 13277415—
SolventWaterHCID 962—
ProductTeniloxazineHCID 6438129—

Reaction Steps

A solution of 22 g of 1-[2-(2-thenyl)phenoxy]-2,3-epoxypropane in 200 ml of ethanol was added to a mixture of 56 g of 2-aminoethyl hydrogen sulfate, 20 g of sodium hydroxide and 20 ml of water with stirring, and the stirring was continued for 4 hours at room temperature. To the mixture containing the intermediate, 2-[3-(2-hydroxy-3-[2-(2-thenyl)phenoxy]propylamino]-ethyl hydrogen sulfate, was added a solution of 40 g of sodium hydroxide in 40 ml of water, and the resulting mixture was stirred for 18 hours on a water bath. To the reaction mixture were added 500 ml of water and 700 ml of toluene. The toluene layer was washed with water and dried over anhydrous sodium sulfate, and the toluene was distilled off under reduced pressure. The oily residue was treated 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-deedbd5090d54afc965c1a988f2985ba
Source noteuspto-grants-1977_01