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Hydrochloric Acid → N-methyl-(1-phenylcyclohexyl)methanamine hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | 1-Phenylcyclohexane-1-carbaldehyde | HCID 14922606 | — |
| 生成物 | N-methyl-(1-phenylcyclohexyl)methanamine | HCID 20803212 | — |
| 生成物 | N-methyl-(1-phenylcyclohexyl)methanamine hydrochloride | HCID 68674577 | 6% |
反応手順
The title compound was synthesized from 1-phenylcyclohexane-carbaldehyde (126 mg, 0.67 mmol) and methyl amine (370 μL, 0.73 mmol, 2.0 M in THF) according to General Procedure H, followed by HCl salt formation. The HCl salt was recrystallized from CH3CN to give pure N-methyl(1-phenylcyclohexyl)methanamine hydrochloride (8 mg, 6%) as colorless crystals. HPLC Rt=7.76 min; 1H NMR (400 mHz, MeOH-d4) 7.43-7.38 (m, 4H), 7.28-7.25 (m, 1H), 3.11 (s, 2H), 2.50 (s, 3H), 2.25-2.22 (m, 2H), 1.67-1.23 (m, 8H); LC-MS 6.37 min, (M+1)+ 204 @ 6.62 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08877975B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-b1fb422ce6cd4e68a85721b51bc0429f |
| 出典メモ | uspto-grants-2014_11 |