HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Indole, 3-acetyl-5-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 5-Nitroindole | HCID 22523 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Indole, 3-acetyl-5-nitro- | HCID 20900 | 99% |
Reaction Steps
A solution of 5-nitroindole (10 g, 61.6 mmol) and acetyl chloride (5.8 g, 74 mmol) in methylene chloride at 0° C. is treated with tin tetrachloride (1M in CH2Cl2, 68 mL), stirred under N2 for 6 h, treated with saturated NaHCO3 to pH 9 and filtered. The filtrate is concentrated in vacuo to give a residue. The residue is dissolved in DMF and filtered. This filtrate is concentrated in vacuo to give the title product, 12.6 g (99% yield), identified by NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951881B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-a82ae2ec0e2041e38687d86285c1a88c |
| Source note | uspto-grants-2005_10 |