HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20310667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20310593 | HCID 20310593 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20310667 | HCID 20310667 | — |
Reaction Steps
A solution of 9-amino-11H-pyrrolo[2,1-b] [3]-benzazepin-11-one in triethyl orthoformate (2.17 g., 10 mmoles in 80 ml.) is refluxed for 5 hrs. The volatiles are removed under vacuum and the residue, dissolved in 100 ml. absolute ethanol is stirred in an ice bath as sodium borohydride (0.88 g., 0.024 moles) is added over a period of 10 minutes. The mixture is stirred for a period of 2 hrs. After concentration of the ethanol, the residue is dissolved in ethyl acetate, washed with water, dried over Na2SO4 and concentrated to dryness to yield 9-methylamino-11H-pyrrolo[2,1-b] [3]benzazepin-11-one as a brown amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04056536 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-a9273035a13145faa457f3d701f03ea6 |
| Source note | uspto-grants-1977_11 |