HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 20296689, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1(3H)-Isobenzofuranone, 4-chloro- | HCID 3040300 | — |
| Reactant | HCID 178449902 | HCID 178449902 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 20296689 | HCID 20296689 | 97% |
Reaction Steps
4-chloroisobenzofuran-1(3H)-one (10 g, 59.32 mmol), (E)-2,2′-(diazene-1,2-diyl)bis(2-methylpropanenitrile) (0.974 g, 5.93 mmol) and 1-bromopyrrolidine-2,5-dione (11.61 g, 65.25 mmol) were dissolved CCl4 (100 mL) and heated at reflux for 2 hours. The reaction was cooled and filtered, the filtrate was evaporated to the desired compound as a yellow gum (14.20 g, 97% yield); 1H NMR (400.132 MHz, CDCl3) δ 7.32 (1H, s), 7.61 (1H, t), 7.73 (1H, d), 7.88 (1H, d); m/z (LC-MS, ESI+), RT=2.28 (M+H not detected).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129380B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-a8e037c0e6624cec8cddb1a406e82aae |
| Source note | uspto-grants-2012_03 |