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Lithium amide → 2,2,6,6-Tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Lithium amide | HCID 24532 | — |
| 反応物 | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| 反応物 | Methyl 2-(2-methylpropane-2-sulfonyl)acetate | HCID 43444477 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2,2,6,6-Tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate | HCID 54332638 | — |
反応手順
38.8 g (0.2 mol) of methyl t-butylsulphonyl-acetate, prepared according to the method of von Leusen and Strating, Rec. Trav, Chim. 84, 140 (1965), and 31.4 g (0.2 mol) of 4-hydroxy-2,2,6,6-tetramethylpiperidine are dissolved in 50 ml of xylene. The mixture is warmed to 130°, 0.2 g of lithium amide in 50 ml of xylene is added and the mixture is stirred for 12 hours at 130°-140°. The xylene is removed in vacuo and the residue is distilled to give 2,2,6,6-tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate; yield: 33.7 grams, boiling point 153°-154°/10-3 mm Hg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04226999 |
| 出典データセット | uspto-grants-1980_10 |
| ORD ID | ord-9a8cddad13b04a89b15fdfef4507ca49 |
| 出典メモ | uspto-grants-1980_10 |