HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 57816840, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 57816839 | HCID 57816839 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57816840 | HCID 57816840 | — |
Reaction Steps
To a solution of the phosphonate prepared in step 2 (300 mg, 0.59 mmol) in CH3CN (5 ml) was added NBS (157 mg, 0.88 mmol) at room temperature. The reaction mixture was stirred at room temperature for 1 h. The solvent was removed and the residue was washed with sat. aq Na2SO3 solution. The aqueous phase was extracted again with DCM. The organic layer was dried over Na2SO4, filtered, concentrated, and purified by prep HPLC on a C18 column, eluting with a gradient of 5-95% CH3CN in H2O as solvent. 1H NMR (CDCl3) δ 1.19-1.27 (m, 6H), δ 3.40 (s, 3H), δ 3.68 (t, 2H), δ 3.84-3.3.88 (m, 1H), δ 3.93-4.10 (m, 8H), δ 4.30-4.36 (m, 4H), δ 6.30 (bs, 2H), δ 6.83-6.97 (m, 3H), δ 7.23-7.28 (m, 2H); MS: 588.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338593B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-a8f078f816d7489e9a167f2d51a1655f |
| Source note | uspto-grants-2012_12 |