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2-(4-Methoxyphenyl)propan-1-amine → N-(2-Chloro-3-trifluoromethylbenzyl)-2-(4-methoxyphenyl)propylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(4-Methoxyphenyl)propan-1-amine | HCID 202625 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 反応物 | 2-Chloro-3-(trifluoromethyl)benzaldehyde | HCID 2736672 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | N-(2-Chloro-3-trifluoromethylbenzyl)-2-(4-methoxyphenyl)propylamine | HCID 69254854 | 77% |
反応手順
A solution of 2-(4-methoxyphenyl)propylamine (183 mg, 1.11 mmole) and 2-chloro-3-trifluoromethylbenzaldehyde (230 mg, 1.11 mmole) in 10 mL of MeOH was treated with a crystal of p-toluenesulfonic acid hydrate, and stirred for 30 minutes. The reaction was diluted with Et2O, and washed with aqueous NaHCO3. The extracts were dried, and the solvent removed. A solution of the residue in 10 mL of MeOH was cooled to 0° and treated with excess NaBH4. The reaction was warmed to 23° and stirred for 30 minutes. The reaction was diluted with H2O and extracted with Et2O. The extracts were washed with H2O, dried and the solvent removed, and gave the titled compound, 305 mg (77% yield). MS (ESI) 358 (MH+)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07365085B2 |
| 出典データセット | uspto-grants-2008_04 |
| ORD ID | ord-186c9854a9884c8eb685c624d6261659 |
| 出典メモ | uspto-grants-2008_04 |