HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Bromo-1H-indole-6-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-bromo-1H-indole-6-carboxylate | HCID 24728007 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-1H-indole-6-carboxylic acid | HCID 24728608 | — |
Reaction Steps
A solution of sodium hydroxide (14.08 g, 352.1 mmol) in water (100 mL) was added a to a solution of 4-bromo-1H-indole-6-carboxylic acid methyl ester in methanol (14.91 mL, 58.7 mmol) at room temperature and stirred for 2.5 hours. The reaction mixture was concentrated in vacuo, 1N HCl was added, and the product was extracted with ethyl acetate to give 13.0 g of 4-bromo-1H-indole-6-carboxylic acid, which was used in the next step with no further purification. 1H NMR (400 MHz, CD3OD) δ 8.13 (t, J=1.0 Hz, 1H), 7.87 (d, J=1.3 Hz, 1H), 7.53 (t, J=3.4 Hz, 1H), 8.13 (d, J=4.2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662824B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-a653a240dae847338270c7b787995551 |
| Source note | uspto-grants-2010_02 |