反応式
Cl[CH2:2][CH2:3][O:4][CH2:5][CH2:6][O:7][CH2:8][CH2:9][OH:10].[CH3:11][NH:12][CH3:13]>>[CH3:11][N:12]([CH3:13])[CH2:2][CH2:3][O:4][CH2:5][CH2:6][O:7][CH2:8][CH2:9][OH:10]参加物
3
実験手順
Commercial Cl(CH2CH2O)3H (abb. ClE3H) (2.0 mole) and dimethylamine (20.0 mole) were mixed in a flask (3.0 l) fitted with a condenser and stirred (RT) for 30 hours. TLC (Si-gel) examination showed the complete consumption of the ClE3H. Excess dimethylamine was removed by two consecutive evaporations under reduced pressure. The residual material was reconstituted in CHCl3, dried (MgSO4), filtered and evaporated to dryness to produce the product, 8-dimethylamino-3,6-dioxaoctanol.
後処理
- customfitted with a condenser
- customthe complete consumption of the ClE3H
- customExcess dimethylamine was removed by two consecutive evaporations under reduced pressure
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated to dryness
出典と根拠
- ORDレコード
- ord-640529c8258d4e74a8dd8c70eedc4121
- 出典データセット
- uspto-grants-1981_04
- 特許番号
- US04263281
関連ノート
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