HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-bromo-6-methyl-1H-indole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-bromo-6-methyl-1H-indole | HCID 24729241 | — |
| Product | 5-bromo-6-methyl-1H-indole-3-carbaldehyde | HCID 82388855 | 85% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Phosphorus oxychloride (0.73 g, 4.79 mmol) and DMF (5.0 mL) were mixed together and stirred for 5 min. A solution of 5-bromo-6-methyl-1H-indole (500 mg, 2.39 mmol) in DMF (3.0 mL) was added to the solution slowly and complete solid was formed which stopped stirring. The solution was adjusted to pH=10 with 1 N NaOH, then heated to 100° C. for 1 min. The reaction was cooled to room temperature. The precipitated solids were filtered and dried to give the title compound (480 mg, 85%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 12.2 (s, 1 H), 9.88 (s, 1 H), 8.28 (s, 1 H), 8.23 (s, 1 H), 7.49 (s, 1 H), 2.44 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394285B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-8f2719acb54b49b0adcbf223c14b6afe |
| Source note | uspto-grants-2016_07 |