HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Ethanone, 1-(2,3-dihydro-5-nitro-1H-indol-1-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Nitroindoline | HCID 36219 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethanone, 1-(2,3-dihydro-5-nitro-1H-indol-1-yl)- | HCID 36566 | — |
Reaction Steps
A mixture of 5-nitroindoline (I, 12.012 g) in pyridine (100 ml) and acetic anhydride (50 ml) is stirred for 17 hr under argon. The mixture is then concentrated under reduced pressure to give the title compound, mp 175°-177°; NMR (CDCl3, 300 MHz) 8.28, 8.10, 8.01, 4.23, 3.31 and 2.28 δ; CMR (CDCl3, 75.47 MHz) 23.95, 27.01, 49.11, 115.73, 119.93, 124.27, 132.4, 143.4 and 169.8 δ; IR (CHCl3) 1680, 1600, 1480, 1470, 1390, 1340 and 1320 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05164510 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-57c24998a7c149c5b442486e85778aa5 |
| Source note | uspto-grants-1992_11 |