HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 68297544, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86714136 | HCID 86714136 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68297544 | HCID 68297544 | 71.1% |
Reaction Steps
MeOH (220 mL) was added to a flask containing 4-(1-phenethylamino-ethylidene)-pent-2-enedioic acid dimethyl ester (7.0 g, 23.1 mmol). NaOMe solution (5.3 mL, 23.1 mmol, 4.375 M in MeOH) and N-bromosuccinimide (4.93 g, 27.7 mmol) were added, and the resulting mixture was refluxed for 1 h. After cooling to r.t., the solvent was evaporated in vacuo. The residue was partitioned between saturated NH4Cl (200 mL) and CH2Cl2 (200 mL). The aqueous layer was extracted with additional CH2Cl2 and the organic layers were combined, dried over MgSO4, and concentrated. The crude product was chromatographed (0-40% EtOAc/hexanes) to give 5.75 g of the title compound as a pale yellow solid. MS: (+) m/z 372.14, 374.16 (M+Na, 79/81Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09271970B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-7dd2223ef0584ea1a0081eda9f8dd83f |
| Source note | uspto-grants-2016_03 |