HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 49766558, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Amino-5-Nitrophenol | HCID 4984721 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 49766558 | HCID 49766558 | — |
Reaction Steps
A solution of 2-amino-5-nitrophenol (97, 24 g, 156 mmol) in CH3CN (1 L) was treated with NBS (28.8 g, 160.8 mmol) at room temperature. After stirring for 1 hour, the solvent was removed to afford brown precipitate, which was taken up with ethyl acetate:hexane (1:1). The precipitate was filtered and was used for the next step without further purification (33 g, 91%). A small amount of sample was purified by column chromatography on silica gel for analysis; 1H NMR (500 MHz, CD3OD): δ 4.93 (brs, 3H), 7.50 (d, 1H, J=2.4 Hz), 7.89 (d, 1H, J=2.4 Hz); 13C NMR (125 MHz, CD3OD): δ 105.5, 108.7, 121.8, 138.5, 143.7, 144.8; HRMS (FAB) calcd for C6H5BrN2O3(M+) 231.9484. found 231.9479.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08093287B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d59f48a27e5b4d25a5d894b43a356078 |
| Source note | uspto-grants-2012_01 |