HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 14126425, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 14126422 | HCID 14126422 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Ethylmorpholine | HCID 7525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14126425 | HCID 14126425 | — |
Reaction Steps
A mixture of 10,11-dihydro-7-hydroxy-11-oxodibenzo[b,f][1,4]thiazepin (4.5g,18.5 mmoles) and lithium aluminum hydride (3.5g,92.5 mmoles) in tetrahydrofuran (200 ml) and N-ethylmorpholine (100 ml) was refluxed for 18 hours. The reaction mixture was decomposed by the addition of 12 ml of a saturated solution of ammonium chloride and 33 ml of lM sodium bicarbonate. The mixture was filtered and the salts were washed with methanol. The filtrate was evaporated to dryness and the residue was extracted several times with ether. Chromatography of the residue on silica gel, eluting with 5% methanol in chloroform, afforded the title compound, m.p. 172°-174°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04728735 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-c42c898ba63a4c33a36d955fa86c0f6c |
| Source note | uspto-grants-1988_03 |