関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | tert-Butanol | HCID 6386 | — |
| 反応物 | Sodium Sulfite | HCID 24437 | — |
| 反応物 | Methyl morpholine oxide | HCID 82029 | — |
| 反応物 | tert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamate | HCID 86635707 | — |
| 触媒 | Osmium | HCID 23937 | — |
| 生成物 | HCID 67270991 | HCID 67270991 | — |
反応手順
To a 250 mL RBF containing tert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamate (105.00 mg, 396 μmol)(mixture of diasteromers at benzylic fluoride stereocenter) was added tert-butanol (3 mL) and water (1 ml). The mixture was allowed to stir at 23° C. for 2 min, then NMO (139 mg, 1187 μmol) and osmium tetraxide (124 μl, 396 μmol) were added and the reaction was allowed to stir for another 48 h. before the reaction was quenched with water and sodium sulfite (1496 mg, 11872 μmol). The reaction was allowed to stir for 15 min and then extracted with EtOAc (3×). The combined organics were washed with HCl (1 N), sodium bicarbonate, brine and dried over sodium sulfate. The dried solution was passed through a plug of silica gel and concentrated to give 102 mg of a colorless oil
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08163909B2 |
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| 出典データセット | uspto-grants-2012_04 |
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| ORD ID | ord-3288873dcc4047e99da710c31337cf04 |
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| 出典メモ | uspto-grants-2012_04 |
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