関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Thiosulfate | HCID 24477 | — |
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | 4-(2-Butynyloxy)-6-methylthiopyrimidine | HCID 22599877 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 4-(2-Butynyloxy)-6-methanesulfonylpyrimidine | HCID 22599863 | — |
反応手順
To 14 ml of chloroform were added 4-(2-butynyloxy)-6-methylthiopyrimidine and 3.5 g of m-chloroperbenzoic acid (>65%), followed by stirring at 0° C. for 10 hours. The reaction mixture was then poured into a saturated aqueous sodium thiosulfate solution and extracted three times with chloroform. The chloroform layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 1.4 g of 4-(2-butynyloxy)-6-methanesulfonylpyrimidine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06838463B2 |
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| 出典データセット | uspto-grants-2005_01 |
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| ORD ID | ord-4fedc6ac9b4648da863d57e9b653d54c |
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| 出典メモ | uspto-grants-2005_01 |
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