関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | Ethyl ketone | HCID 7288 | — |
| 生成物 | 1-Hydroxy-2-methyl-1-phenyl-3-pentanone | HCID 546017 | 72% |
反応手順
50 mmol (5.1 ml) of benzaldehyde are added at -78° C. to the manganous enolate of diethyl ketone, prepared by the procedure described above. After stirring for 10 seconds at -78° C., the reaction medium is hydroIyzed by the dropwise addition of a saturated solution of (NH4)2SO4. After decantation, filtration on hyflo-supercel and evaporation of the solvents under vacuum, 5-phenyl-5-hydroxy-4-methylpentan-3-one is isolated by low pressure liquid chromatography on 15 μm silica gel using cyclohexane/ethyl acetate (90/10) as the eluent. Yield=72%. Erythro/threo=61/39.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05426201 |
|---|
| 出典データセット | uspto-grants-1995_06 |
|---|
| ORD ID | ord-eb2ffed42db34070991af4f46a60fd88 |
|---|
| 出典メモ | uspto-grants-1995_06 |
|---|