HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Bromo-4-nitrophenyl)acetic acid → HCID 12404389, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Bromo-4-nitrophenyl)acetic acid | HCID 12404388 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 12404389 | HCID 12404389 | — |
Reaction Steps
A solution of (2-bromo-4-nitrophenyl)acetic acid (500 mg, 2 mmol) in 11 mL of concentrated ammonium hydroxide was added a solution of FeSO4.7H2O (3.4 g, 12 mmol) in 11 mL of water over 5 minutes, and then the mixture was heated to reflux for 1 hour. Cooled to ambient temperature, filtered off solids and the filtrate was adjusted to pH to 5 with 2N HCl. Extracted with EtOAc and combined organic layers were washed with water, dried over anhydrous sodium sulfate, and concentrated to get (4-amino-2-bromophenyl)acetic acid. 1H-NMR (300 MHz, CDCl3) δ ppm 7.01 (d, J=8.0 Hz, 1H), 6.92 (d, J=2.0 Hz, 1H), 6.62 (dd, J=2.5 Hz, 1H), 3.61 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056859B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-953dc95a5762439fb61d8f5fe8a545d2 |
| Source note | uspto-grants-2015_06 |