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1,3-Dibromopropane → (3-Bromo-propyl)-(2-chloro4,6-dimethyl-phenyl)-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,3-Dibromopropane | HCID 8001 | — |
| 反応物 | 2-Chloro-4,6-dimethylaniline | HCID 113033 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | (3-Bromo-propyl)-(2-chloro4,6-dimethyl-phenyl)-amine | HCID 21916144 | 67.1% |
反応手順
To a solution of the 2-chloro-4,6-dimethyl aniline (16.9 g g, 108 mmol) in 1,4-dioxane (80 mL) was added n-butyl lithium solution (2.5 M in hexanes, 48 mL), dropwise, at 0° C. under argon. The reaction mixture was warmed up to rt and stirred for 20 min. 1,3-Dibromopropane (109 g, 543 mmol) was added and the reaction mixture was stirred overnight. The mixture was filtered through celite and concentrated. Purification was carried out by reverse phase chromatography using water, methanol and trifluoroacetic acid to obtain product (20.01 g, 72.5 mmol, 67%) as brown oil. LC/MS: tR=1.5 min. [M+H] 277. 1H NMR (CD3OD) δ: 7.12 (s, 1H), 6.99 (s, 1H), 3.52 (t, J=6.65 Hz, 2H), 3.36 (t, J=6.75 Hz, 2H), 2.36 (s, 3H), 2.29 (s, 3H), 2.14 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07238699B2 |
| 出典データセット | uspto-grants-2007_07 |
| ORD ID | ord-37c9ceb21e4d4abc8d8fe587992375b2 |
| 出典メモ | uspto-grants-2007_07 |