HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Bromo-1-(3-phenyl-2,3-dihydro-1H-indol-1-yl)propan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromopropanoyl chloride | HCID 97980 | — |
| Reactant | 3-phenyl-2,3-dihydro-1H-indole | HCID 10932353 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Bromo-1-(3-phenyl-2,3-dihydro-1H-indol-1-yl)propan-1-one | HCID 21320461 | 96.6% |
Reaction Steps
A solution of 3.0 g of 2-bromopropionylchloride in 5 ml of benzene was added dropwise at 10° C. to a mixture of 3.0 g of 3-phenylindoline, 3.0 ml of triethylamine in 30 ml of dry benzene. The mixture was then washed with water, the benzene layer dried over sodium sulfate and the solvent removed in vacuo at room temperature to leave 4.9 g of the desired N-(2-bromopropionyl)-3-phenylindoline as a resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04153789 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-4a59b7c62f2043449ee9658555c1c9b5 |
| Source note | uspto-grants-1979_05 |