HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indole-3-propanoic acid → 1H-Indole-3-propanamide, N-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indole-3-propanoic acid | HCID 3744 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1H-Indole-3-propanamide, N-methyl- | HCID 7661699 | — |
Reaction Steps
A mixture of 57 g trifluoroacetic acid and 105 g trifluoroacetic anhydride in 400 ml anhydrous acetonitrile are added dropwise to a stirred suspension of 95.1 g 3-(3-indolyl)propionic acid in 500 ml anhydrous acetonitrile and maintained with stirring at -15° for 30 minutes. Under good cooling 500 ml anhydrous pyridine are added between -20° and -15° and quickly 238 ml of a 4.2 N solution of anhydrous methylamine in acetonitrile. The mixture is warmed with stirring at 0° for 15 minutes and maintained to 0° for 3 hours. 3-(3-indolyl)-N-methyl-propionamide (M.pt 97°-98° after crystallization from methylene chloride/ethyl acetate) is obtained after working up.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04350634 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-44ebba0332634fb99e3376d1110cf41c |
| Source note | uspto-grants-1982_09 |