HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → HCID 22247313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Acetyl-3-(2-hydroxyethyl)-4,6-dimethylindoline | HCID 22247316 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22247313 | HCID 22247313 | 61.1% |
Reaction Steps
1-Acetyl-3-(2-hydroxyethyl)-4,6-dimethylindoline (7.0 g) and CBr4 (9.9 g) were dissolved in CH3CN (70 ml), and Ph3P (9.4 g) was added, which was followed by stirring at room temperature for 30 min. CH3CN was evaporated under reduced pressure. AcOEt (100 ml) was added, and the mixture was washed with water and dried over anhydrous sodium sulfate. AcOEt was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: benzene/AcOEt=50/1-10/1) to give 5.4 g of 1-acetyl-3-(2-bromoethyl)-4,6-dimethyl-indoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06200988B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-bb74fa7a031742c8abbfd0b352076fe0 |
| Source note | uspto-grants-2001_03 |