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Triethylamine → 3-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-N-tricyclo[3.3.1.13,7]dec-1-ylpropanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2,6-Di-tert-butyl-4-mercaptophenol | HCID 70370 | — |
| 反応物 | N-(Adamantan-1-yl)prop-2-enimidic acid | HCID 284637 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-N-tricyclo[3.3.1.13,7]dec-1-ylpropanamide | HCID 14986564 | — |
反応手順
Following the method of Example 4, 2,6-bis(1,1-dimethylethyl)-4-mercaptophenol (1.19 g, 0.005 mole), the title compound of Example 5 (1.03 g, 0.005 mole) and triethylamine (0.5 ml) were stirred in methanol (100 ml) for 12 hours at room temperature under argon. The solvent and triethylamine were removed on a rotary evaporator and the product purified by chromatography on silica, recrystallized from ethyl aceate/hexane, filtered and dried in vacuo, m.p. ca. 172.5°-173.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05157053 |
| 出典データセット | uspto-grants-1992_10 |
| ORD ID | ord-b19c1f6cb3bb40d185dfbc392d006638 |
| 出典メモ | uspto-grants-1992_10 |