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Dichloroacetyl chloride → 2-(Dichloroacetyl)-1-(1-methylethyl)-4-methyl-1,2,3,4-tetrahydro-isoquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloroacetyl chloride | HCID 6593 | — |
| 反応物 | Isoquinoline | HCID 8405 | — |
| 反応物 | 2-Phenylpropylamine | HCID 11398 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Isobutyryl chloride | HCID 62325 | — |
| 反応物 | 4-Methyl-1,2,3,4-tetrahydroisoquinoline | HCID 13738934 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(Dichloroacetyl)-1-(1-methylethyl)-4-methyl-1,2,3,4-tetrahydro-isoquinoline | HCID 20133043 | — |
反応手順
By procedures described in Example 1 (Method A), β-methyl-phenethylamine and isobutyryl chloride were converted to -4-methyl-1,2,3,4-tetrahydroisoquinoline. A reaction vessel was charged with 3.0 g of this isoquinoline compound, 10 ml 10% sodium hydroxide and 50 ml methylene chloride. With this mixture stirred, 2 ml dichloroacetyl chloride was added dropwise to the mixture. The mixture was stirred for 2 minutes, then water was added. The organic extract was dried with magnesium sulfate and stripped of solvent. The residue was recrystallized from aqueous ethanol to provide 4 g of a white needle-crystalline 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-451cd1213c07448ab4fd623420318f8e |
| 出典メモ | uspto-grants-1988_07 |