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Benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate → 1-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)piperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate | HCID 58812409 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)piperazine | HCID 58299824 | 88% |
反応手順
A mixture of benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate (Method 90, 2.1 g, 5.55 mmol) and Pd/C (0.059 g, 0.55 mmol) in methanol (30 mL) was stirred under H2 (g) for 24 hours. The reaction mixture was filtered through a pad of Celite and concentrated under reduced pressure to give 1.20 g, (88%) of a yellow oil. 1H NMR: CD3Cl 3.74 (t, 2H), 2.90 (m, 4H), 2.51 (m, 6H), 0.88 (s, 9H), 0.04 (s, 6H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07723337B2 |
| 出典データセット | uspto-grants-2010_05 |
| ORD ID | ord-598620f990ba4d77a236db01de1f2e4d |
| 出典メモ | uspto-grants-2010_05 |