関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Triphenylsulfonium Bromide | HCID 11984010 | — |
| 反応物 | (Adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid triethylammonium salt | HCID 131731910 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Triphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonate | HCID 44224732 | 92% |
反応手順
Within a 1-L three-neck flask, 100 g (purity: 93%, 219 mmol, 1.0 eq) of the (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid triethylammonium salt obtained in Example 1-c was dissolved in 300 g of chloroform. To the resulting solution, 250 g of water and 78.9 g (223 mmol, 1.05 eq) of triphenylsulfonium bromide were added. This reaction solution was stirred for 1 hour. After the reaction, the reaction solution was separated into an organic layer and an aqueous layer. The organic layer was washed with water, followed by distillating chloroform from the washed organic layer. The thus-obtained concentrated solution was dissolved in a mixed solvent of chloroform, ethyl acetate and diisopropyl ether and then recrystallized. With this, 119 g of target triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate was obtained (yield: 92%, purity: 99%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846966B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-d6bb2c220ef44b70a03283ff2acd87a6 |
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| 出典メモ | uspto-grants-2014_09 |
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