Methylamine → (3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amine
反応式
[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][CH:2]1[CH:7]=O.[CH3:9][NH2:10].[H][H]>O1CCCC1>[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][CH:2]1[CH2:7][NH:10][CH3:9]参加物
反応条件
- 温度
- 100 °C
実験手順
3,4-Dihydro-2H-pyran-2-carbaldehyde (300 g, 2.68 mol) was dissolved in tetrahydrofuran (710 mL). Raney-Co catalyst (30 g, tetrahydrofuran moist) was added. Gaseous methyl amine (415.4 g, 13.4 mol) was transferred into the solution within 50 minutes (45° C.). Hydrogen (49.2 L) was added and the pressure adjusted to 100 bar and the solution was stirred for about 2 h at 100° C. The reaction vessel was cooled to room temperature, the gas removed and the solution degassed. The solution was concentrated under reduced pressure. The crude product (344.5 g) was distilled at reduced pressure to receive (3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amine (289.8 g, 2.28 mol, 85% yield). Analytical data amine (3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amine: Bp. 55-57° C. at 16 mbar; HPLC-MS: (M+H)+=128 at rt=0.619 min. (TIC), rt=0.596 min. (UV), rt=0.631 min. (ELS), Chromolith SpeedROD RP-18e 50-4.6 mm, solvent A: water+0.1% TFA, solvent B: acetonitrile+0.1% TFA, gradient: 4% solvent B at 0.0 min., 100% solvent B at 2.6 min., flow: 2.4 mL/min., UV: 220 nm.
後処理
- custom(45° C.)
- temperatureThe reaction vessel was cooled to room temperature
- customthe gas removed
- customthe solution degassed
- concentrationThe solution was concentrated under reduced pressure
- distillationThe crude product (344.5 g) was distilled at reduced pressure
出典と根拠
- ORDレコード
- ord-8b465595288a40ba984c52f2b05e8ace
- 出典データセット
- uspto-grants-2012_10
- 特許番号
- US08278454B2
反応ノート
読み込み中…