化工社化工社 化学情報印刷レポート · 研究参考用
Phenethylamine → 2-(Dichloroacetyl)-1-phenyl-1,2,3,4-tetrahydroisoquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phenethylamine | HCID 1001 | — |
| 反応物 | Dichloroacetyl chloride | HCID 6593 | — |
| 反応物 | Benzoyl chloride | HCID 7412 | — |
| 反応物 | Isoquinoline | HCID 8405 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1,2,3,4-Tetrahydro-1-phenylisoquinoline | HCID 100137 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(Dichloroacetyl)-1-phenyl-1,2,3,4-tetrahydroisoquinoline | HCID 20133033 | — |
反応手順
By procedures described in Example 1 (Method A), phenethylamine and benzoyl chloride were converted to 1-phenyl-1,2,3,4-tetrahydroisoquinoline. A reaction vessel was charged with 3.5 g of this isoquinoline compound, 10 ml 10% sodium hydroxide and 50 ml methylene chloride. With this mixture stirred, 1.2 ml dichloroacetyl chloride was added dropwise to the mixture. The mixture was stirred for 10 minutes, then water was added. The organic extract was dried with magnesium sulfate and stripped of solvent. The residue was recrystallized from ethanol to provide 4 g of a white cubic-crystal product having the elemental analysis reported in Table I.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04755218 |
| 出典データセット | uspto-grants-1988_07 |
| ORD ID | ord-12abee4c4ac9483ca98270db7029d4fa |
| 出典メモ | uspto-grants-1988_07 |