HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 53861417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | 9-Chloro-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepin-6-ol | HCID 13338333 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53861417 | HCID 53861417 | 76% |
Reaction Steps
A 35% dispersion of potassium hydride in mineral oil (2.6 g, 23 mmol) in dimethylformamide (40 ml) was stirred and treated with 9-chloro-2,3,4,5-tetrahydro-3-methyl-1H-3-benzazepin-6-ol (4.0 g, 19 mmol), stirred for 20 minutes, treated with ethyl bromoacetate (3.8 g, 23 mmol) and stirred for 72 hours. The mixture was concentrated, partitioned between water and methylene chloride and the organic phase was washed, dried with magnesium sulfate and concentrated. The residue was chromatographed on silica gel eluted with methanol-methylene chloride (8:92) to give 4.3 g of ethyl [(9-chloro-2,3,4,5-tetrahydro-3-methyl-1H-3-benzazepin-6-yl)oxy]acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05639748 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-8c6351e952dd4a23978145d5122f121a |
| Source note | uspto-grants-1997_06 |