反応式
[H-].[Na+].[NH2:3][C:4]([CH3:10])([CH2:7][O:8][CH3:9])[CH2:5][OH:6].IC.[CH3:13]CO>CCOCC>[CH3:9][O:8][CH2:7][C:4]([NH2:3])([CH2:5][O:6][CH3:13])[CH3:10]参加物
実験手順
To a 3-necked 3 L RB flask equipped with overhead stirrer, condenser and N2 inlet line was added NaH (Morton Thiokol, Inc.-Alfa Products, 60% in mineral oil, 44 g, 1.1 mol). After washing with hexane (3×200 mL), dry THF (1.1 L) was added to the flask. After cooling to 0°, 2-amino-3-methoxy-2-methyl-1-propanol (61C, 119.16 g, 1.0 mol) was added dropwise to the flask at such a rate that the reaction temperature remained below 30°. The resulting slurry was cooled to 0°. Iodomethane (Aldrich, 141.94 g, 1.0 mol, 62.25 mL) was added dropwise to the mixture at such a rate that the reaction temperature remained below 30°. After the mixture was stirred for 1 h, EtOH (25 mL) was added to quench the reaction. The volume of the reaction was reduced to 200 mL. This material was diluted to 2 L with Et2O, filtered and the solvent removed. Fractional distillation of this material gave 91.02 g (68.3% yield of 1,1-bis-(methoxymethyl)ethylamine, bp 146°-149°, (C,H,N).
後処理
- customTo a 3-necked 3 L RB flask equipped with overhead stirrer, condenser and N2 inlet line
- washAfter washing with hexane (3×200 mL), dry THF (1.1 L)
- additionwas added to the flask
- temperatureAfter cooling to 0°
- customremained below 30°
- temperatureThe resulting slurry was cooled to 0°
- customremained below 30°
- customto quench
- customthe reaction
- filtrationfiltered
- customthe solvent removed
- distillationFractional distillation of this material
出典と根拠
- ORDレコード
- ord-228811dfa8744e98b1bf471af6944c9a
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US04999369
関連ノート
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