HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → (S)-2-((R)-2-(4-Fluoro-3-methylphenyl)-2-methoxyethyl)-N-hydroxypent-4-enamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | (S)-Methyl 2-((R)-2-(4-fluoro-3-methylphenyl)-2-methoxyethyl)pent-4-enoate | HCID 59568824 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (S)-2-((R)-2-(4-Fluoro-3-methylphenyl)-2-methoxyethyl)-N-hydroxypent-4-enamide | HCID 59568790 | — |
Reaction Steps
(S)-Methyl 2-((R)-2-(4-fluoro-3-methylphenyl)-2-methoxyethyl)pent-4-enoate (50 mg) was dissolved into 1 mL of a mixture of THF, methanol, and 50% NH2OH in H2O (2:2:1) and to this solution was added 2 mg KCN. The reaction was stirred for 3 days at room temperature and then quenched by the addition of 1M HCl (10 mL). The mixture was extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with brine (2×10 mL) before being concentrated under reduced pressure. The product was isolated by flash column chromatography eluting with 0% to 10% methanol/DCM to obtain the title compound (34 mg) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119692B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-4696ee3eb0d7433dacfa4d627db1b57b |
| Source note | uspto-grants-2012_02 |