HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Acetyl-2,3-dihydro-1H-indol-5-yl)propan-1-one → HCID 20094393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Acetyl-2,3-dihydro-1H-indol-5-yl)propan-1-one | HCID 23003971 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20094393 | HCID 20094393 | 79.1% |
Reaction Steps
To a solution of 1-acetyl-5-propionylindoline (1.65 g) in tetrahydrofuran (150 ml) were added concentrated sulfuric acid (5 drops) and pyrrolidone hydrotribromide (4.14 g), and the mixture was stirred at room temperature for 16 hours. The insoluble materials were filtered off, and the filtrate was concentrated under reduced pressure. The residue was extracted with ethyl acetate, and the extract was washed with water, dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was recrystallized from ethanol to give 1.78 g of 1-acetyl-5-(2-bromopropionyl)indoline melting at 140°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05387603 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-f18b0b7521a6488896d1ec2f879e7208 |
| Source note | uspto-grants-1995_02 |