関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Sulfite | HCID 24437 | — |
| 反応物 | Methyl morpholine oxide | HCID 82029 | — |
| 反応物 | (1-Allylcyclobutoxy)(tert-butyl)dimethylsilane | HCID 66844818 | — |
| 反応物 | 2-Methylpropan-2-ol--water (1/1) | HCID 71401949 | — |
| 触媒 | Osmium Tetroxide | HCID 30318 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol | HCID 66845148 | — |
反応手順
To a 2 L round bottomed flask was added (1-allylcyclobutoxy) (tert-butyl)dimethylsilane (previous step) and H2O/t-BuOH (1:1, 1 L). NMO (32.68 g, 279 mmol) was added to the mixture. After stirring for 5 min the solution was found to be homogenous. Osmium tetroxide (1.00 g, 3.93 mmol) was added and the reaction was stirred at RT. After 2 h, TLC revealed the reaction to be complete. 500 mL of H2O and sodium sulfite (19.5 g, 155 mmol) were added and the reaction was stirred for another hour. The aqueous solution was extracted with ether (2×1 L). The combined organics were concentrated in vacuo to give 3-(1-(tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol, as a light yellow oil. The oil contained some t-BuOH, but was carried forward without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07872009B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-aa5b1e4ea92b4414a0676c8fc3e8f0ff |
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| 出典メモ | uspto-grants-2011_01 |
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