HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 7,7-Di-pyridin-2-yl-hept-6-enoic acid hydroxyamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 7,7-Di-pyridin-2-yl-hept-6-enoic acid | HCID 58545062 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 7,7-Di-pyridin-2-yl-hept-6-enoic acid hydroxyamide | HCID 46852304 | — |
Reaction Steps
HONH2 (50% aqueous, 0.3 mL) was added to IV (32 mg, 0.1 mmol) in DMF (0.3 mL) and THF (0.3 mL) at 0° C. The reaction mixture was stirred at it for 17 h, after which brine (3 mL) and EtOAc (3 mL) were added. The phases were separated, and the aqueous phase was extracted with EtOAc (2×3 mL). The organic phases were then combined, dried over MgSO4, filtered, and subsequently evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using CH2Cl2/MeOH (100:3 to 100:10) as eluant to furnish V, a colourless oil (9.6 mg, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748458B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-3c2a8810ba2f4e9ea9b6eee5b715666b |
| Source note | uspto-grants-2014_06 |