HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (7-Nitroindol-1-yl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | methyl 2-(7-nitro-1H-indol-1-yl)acetate | HCID 86681614 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7-Nitroindol-1-yl)-acetic acid | HCID 68424240 | 95% |
Reaction Steps
To a solution of methyl 2-(7-nitro-1H-indol-1-yl)acetate (0.37 g, 1.580 mmol) in THF (20 ml), LiOH 1N (3.16 ml, 3.16 mmol) was added at room temperature. The reaction was stirred at the same temperature for 16 hours. Aqueous 2N HCl was added and the solvent was partially removed under vacuum. The remaining aqueous phase was extracted with ethyl acetate; the organic phase was dried over sodium sulfate and the solvent was evaporated under vacuum affording 2-(7-nitro-1H-indol-1-yl)acetic acid (0.33 g, 1.499 mmol, 95% yield). MS/ESI+ 220.9 [MH]+. This compound was used without any additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024027B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-ac45c9b0380145d2bf04389534a6b83b |
| Source note | uspto-grants-2015_05 |