Methylamine → HCID 59277580、化合物
反応式
[CH3:1][NH2:2].[CH2:3]([O:6][C:7]1[C:14]([O:15][C:16]([F:19])([F:18])[F:17])=[CH:13][CH:12]=[CH:11][C:8]=1[CH:9]=O)[CH2:4][CH3:5].[BH4-].[Na+]>CO>[CH3:1][NH:2][CH2:9][C:8]1[CH:11]=[CH:12][CH:13]=[C:14]([O:15][C:16]([F:19])([F:18])[F:17])[C:7]=1[O:6][CH2:3][CH2:4][CH3:5]参加物
実験手順
A solution of methylamine (19 mL of a 2.0 M solution in MeOH, 38 mmol) was added to 2-propoxy-3-trifluoromethoxybenzaldehyde (1.15 g, 4.60 mmol). The mixture was stirred for 18 h. The solution was concentrated under reduced pressure. The resulting clear oil was dissolved in EtOH (19 mL) and treated with NaBH4 (0.174 g, 4.60 mmol). After stirring for 5.5 h, the reaction mixture was concentrated under reduced pressure, then dissolved in 1 N NaOH (19 mL). The mixture was extracted with Et2O (3×50 mL). The organics were collected, washed with brine (2×100 mL), dried (Na2SO4) and concentrated to yield the title compound (0.89 g, 73%) as an orange oil: 1H NMR (300 MHz, DMSO-d6) δ 7.41 (dd, J=7.7, 1.6 Hz, 1H), 7.25 (dd, J=6.7, 1.3 Hz, 1H), 7.16 (t, J=7.7 Hz, 1H), 3.87 (t, J=6.3 Hz, 2H), 3.68 (s, 2H), 2.27 (s, 3H), 2.07 (br s, 1H), 1.74 (q, J=6.4 Hz, 2H), 1.02 (t, J=3.1 Hz, 3H).
後処理
- concentrationThe solution was concentrated under reduced pressure
- dissolutionThe resulting clear oil was dissolved in EtOH (19 mL)
- stirringAfter stirring for 5.5 h
- concentrationthe reaction mixture was concentrated under reduced pressure
- dissolutiondissolved in 1 N NaOH (19 mL)
- extractionThe mixture was extracted with Et2O (3×50 mL)
- customThe organics were collected
- washwashed with brine (2×100 mL)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-1e49c290dc2c4a6eaf41cd8ed5f3681a
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07879872B2
反応ノート
読み込み中…