HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 13316668, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13316665 | HCID 13316665 | — |
| Product | HCID 13316668 | HCID 13316668 | — |
Reaction Steps
3.1 gm (0.007 mol) of 1-[7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-(2-{3,4-dimethoxy-phenyl}-ethyl)-amino]-propane were refluxed for 21 hours with 1.0 gm (0.007 mol) of potassium carbonate and 0.6 ml (0.007 mol) of allyl bromide in 100 ml of chloroform. Subsequently, the organic phase was extracted with water, dried, evaporated in vacuo, and the residue was purified on an aluminum oxide column (300 gm neutral, activity III) with methylene chloride containing 2% of acetone as the eluant. Subsequently the hydrochloride was precipitated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490369 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-9fecd3d26ad246afb75b32c5f45992c5 |
| Source note | uspto-grants-1984_12 |