HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20310625, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13152894 | HCID 13152894 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20310625 | HCID 20310625 | — |
Reaction Steps
A solution of 9amino-6,11-dihydro-5H-pyrrolo-[2,1-b][3]benzazepin-11-one in triethyl orthoformate (2.14 g.; 10 mmoles in 80 ml) is refluxed for 5 hours. The volatiles are removed under vacuum and the residue dissolved in 100 ml. of 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 hours. 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 -6,11 -dihydro-5H-pyrrolo-[2,1-b][3]benzazepin-11-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075225 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-8cf88d4758e3400b890635dced475154 |
| Source note | uspto-grants-1978_02 |