関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium Dithionite | HCID 24489 | — |
| 反応物 | Methyl morpholine oxide | HCID 82029 | — |
| 反応物 | HCID 178440188 | HCID 178440188 | — |
| 触媒 | Osmium Tetroxide | HCID 30318 | — |
| 溶媒 | t-Butanol tetrahydrofuran water | HCID 22124471 | — |
| 生成物 | HCID 178443794 | HCID 178443794 | — |
反応手順
A mixture of diisopropyl E-3(1-trityl-1,2,4-triazol-3-yl)prop-2-ene phosphonate (10.31 g, prepared as described in Example 15), N-methyl-morpholine N-oxide (4.69 g) and osmium tetroxide (2.5 ml, 2.5% in t-butanol) in t-butanol-tetrahydrofuran-water (10:3:1, 350 ml) was stirred at room temperature, under nitrogen, for eight hours. Sodium dithionite (10 g) and water (75 ml) were added, the mixture stirred for thirty minutes, filtered and evaporated under reduced pressure. The residue was made weakly acidic with 2M hydrochloric acid, then partitioned between ethyl acetate and brine. The aqueous layer was reextracted with ethyl acetate and the combined organic layers washed with brine, dried over magnesium sulphate and evaporated under reduced pressure. Chromatography on silica, using dichloromethane-ethanol (12:1) as eluant, gave diisopropyl (2RS,3SR)-2,3-dihydroxy-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (8.46 g, m.p. 148°-151° C.), 99% pure by GC. NMR (CDCl3): δ1.3(12H,m), 1.88-2.15(2H,m), 3.7(1 H,d), 4.13(1H,d), 4.33(1H,m), 4.6-4.8(3H,m), 7.1-7.4(15H,m), 7.95(1H,s). EI M/S: M+ 549. CI M/S: MH+ 550.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05393732 |
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| 出典データセット | uspto-grants-1995_02 |
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| ORD ID | ord-d169318914374fceaccd592986e99669 |
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| 出典メモ | uspto-grants-1995_02 |
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