HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 12459834, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2,4-dimethoxy-6-methylbenzoate | HCID 601782 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 12459834 | HCID 12459834 | 82.1% |
Reaction Steps
Dissolve compound 3 (10 g, 0.0476 mol) in 50 ml carbon tetrachloride, heat to reflux under nitrogen protection, add portion wise a mixture of NBS (8.5 g, 0.0476 mol) and BPO (0.11 g, 0.476 mmol), after finishing the addition, reflux to react for 1 h. Then stop the reaction, cool and filter the mixture, spin-dry filtrate to obtain a pale yellow solid, re-crystallize from ethanol to obtain 11.3 g white solid (82%). 1H-NMR (400M, CDCl3) δ (ppm): 3.85 (s, 3H), 3.93 (s, 3H), 3.96 (s, 3H), 4.66 (s, 2H), 6.47 (s, 1H), 6.74 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359298B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-47bfdebc3080426bbd98248811b517ee |
| Source note | uspto-grants-2016_06 |