Methyl sulfate(1-) → 3-Butyl-5-methyl-1,3,5-oxadiazinane-2,4,6-trione
反応式
S([O-])(O[CH3:5])(=O)=O.[CH2:7]([N:11]1[C:16](=[O:17])[NH:15][C:14](=[O:18])[O:13][C:12]1=[O:19])[CH2:8][CH2:9][CH3:10].C([N+](CCCC)(CCCC)CC1C=CC=CC=1)CCC>>[CH2:7]([N:11]1[C:16](=[O:17])[N:15]([CH3:5])[C:14](=[O:18])[O:13][C:12]1=[O:19])[CH2:8][CH2:9][CH3:10]参加物
3
実験手順
The process described in example 14 is carried out without distillation of the solvent. 72 g of methyl sulfate (0.57 mole) are added to the solution of the salt of tributylbenzylammonium 3-butyl-1,3,5-oxadiazine-2,4,6-trione. The solvent is evaporated after 5 hours of reaction at 25° C. The solid residue is washed with water and with carbon tetrachloride. 88 g of 3-butyl-5-methyl-1,3,5-oxadiazine-2,4,6-trione (yield: 81%) of the formula (II) are obtained.
後処理
- distillationis carried out without distillation of the solvent
- customThe solvent is evaporated after 5 hours of reaction at 25° C
- washThe solid residue is washed with water and with carbon tetrachloride
出典と根拠
- ORDレコード
- ord-3a55517be56f445a955b32360eaa0397
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04544743
反応ノート
読み込み中…