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Diisopropyl Ether → 5-(p-Tolyl)thianthrenium nonafluorobutanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropyl Ether | HCID 7914 | — |
| 反応物 | Trifluoroacetic anhydride | HCID 9845 | — |
| 反応物 | Perfluorobutanesulfonic acid | HCID 67815 | — |
| 反応物 | Thianthrene, 5-oxide | HCID 73220 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5-(p-Tolyl)thianthrenium nonafluorobutanesulfonate | HCID 23137824 | — |
反応手順
In 10 ml of toluene was dissolved 2 g of thianthrene-S-oxide and the solution was cooled with ice. Then, 2.8 ml of trifluoroacetic anhydride and 1.2 ml of nonafluorobutanesulfonic acid were added thereto, followed by stirring for one hour. Diisopropyl ether was added thereto and the supernatant solution was removed. The residue was purified by a silica gel column (chloroform/methanol=19/1) to obtain 4.4 g of 5-(p-tolyl)thianthrenium nonafluorobutanesulfonate. 1H-NMR (400 MHz, CDCl3): σ 2.34 (s, 3H), 7.08 (d, 2H), 7.22 (d, 2H), 7.78 (m, 6H), 8.65 (d, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07615330B2 |
| 出典データセット | uspto-grants-2009_11 |
| ORD ID | ord-fe3cbaa672e540b292fbcce13e566fe5 |
| 出典メモ | uspto-grants-2009_11 |