HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → methyl 5-bromo-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 5-Bromo-1H-indole-2-carboxylic acid | HCID 252137 | — |
| Product | methyl 5-bromo-1H-indole-2-carboxylate | HCID 914343 | — |
Reaction Steps
A solution of 5-Bromo-1H-indole-2-carboxylic acid (commercial, 10.0 g, 41.6 mmol) in methanol (200 ml) was cooled to 0° C. and saturated with HCl (g). The resulting solution was allowed to warm gradually to room temperature overnight. The solvent was removed in vacuo and the residue treated with 0.88 ammonia (500 ml). The resulting solution was extracted with dichloromethane (3-fold 150 ml) and the combined organics dried (magnesium sulphate) and the solvent removed in vacuo to give the required product as a colourless oil (8.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183294B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-6e23edc77f854fb0a5ce3f14c9c8efb3 |
| Source note | uspto-grants-2007_02 |