HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl bromide → HCID 12833523, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | Fenoldopam monohydrobromide | HCID 11957552 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 12833523 | HCID 12833523 | — |
Reaction Steps
6-Chloro-7,8-dihydroxyl-1-p-hydroxyphenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide (Example 2, 1.0 g) was slurried in 200 ml of trifluoroacetic acid, then 1.29 ml of acetyl bromide was added. The mixture was heated at reflux for 2 hours then stirred for 2 hours. After evaporation to dryness the residue was taken up in benzene and concentrated to give a solid which was recrystallized from ethylacetatehexane to give 6-chloro-7,8-diacetoxy-1-(p-acetoxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide; m.p. 214.5-217°, 0.77 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04197297 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-171e7b85a133411dbfd9ac20622b877c |
| Source note | uspto-grants-1980_04 |