HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl chloride → HCID 14032992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 70054036 | HCID 70054036 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14032992 | HCID 14032992 | — |
Reaction Steps
Bromoacetyl chloride (28.3 g) is added dropwise to a suspension of N-methyl-tetrahydroquinolin-2-one (14.7 g) and AlCl3 (26.7 g) in methylene chloride (400 ml), and the reaction mixture is refluxed for 5 hours. The reaction mixture is cooled to RT, stirred with an ice/water mixture for 30 minutes, diluted with methylene chloride (200 ml) and separated. The aqueous layer is extracted with methylene chloride, and the combined organic extracts are washed with H2O, dried, filtered and concentrated in vacuo, yielding a crude solid which is recrystallized from isopropanol affording the desired product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04818755 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-f66d923ad19540698fc541ed04eb1bef |
| Source note | uspto-grants-1989_04 |