Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aminoethyl sulfate | HCID 70223 | — |
| Reactant | 2-({2-[(Thiophen-2-yl)methyl]phenoxy}methyl)oxirane | HCID 13277415 | — |
| Solvent | Water | HCID 962 | — |
| Product | Teniloxazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04005084 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-deedbd5090d54afc965c1a988f2985ba |
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| Source note | uspto-grants-1977_01 |
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