HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → benzyl 4-(1H-indol-3-yl)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Indole-3-Butyric Acid | HCID 8617 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | benzyl 4-(1H-indol-3-yl)butanoate | HCID 1482096 | 94.1% |
Reaction Steps
To a solution of 3-indolebutyric acid (25 g) and potassium carbonate (20 g) in dimethylformamide (150 ml) was added benzylbromide (21 g) at room temperature. After stirring for 4 hours, the mixture was poured into ice and diluted hydrochloric acid (300 ml). The organic layer was extracted with ethyl acetate (150 ml), and the extract was washed with water (150 ml×3) and dried over magnesium sulfate. After the solvent was removed in vacuo, the residue was crystallized from n-hexane to give a solid of benzyl 4-(3-indolyl)butyrate (33.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05283251 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-0a00b4a574234698b32465914e367558 |
| Source note | uspto-grants-1994_02 |