反応式
[Cl:1][C:2]([Cl:8])([Cl:7])[C:3]([CH3:6])([OH:5])[CH3:4].[Cl:9][C:10]([CH3:16])([CH3:15])[C:11]([O:13][CH3:14])=[O:12]>>[C:11]([O:13][CH3:14])(=[O:12])[C:10]([CH3:16])=[CH2:15].[C:11]([OH:13])(=[O:12])[C:10]([CH3:16])=[CH2:15].[C:11]([O:5][C:3]([CH3:6])([CH3:4])[C:2]([Cl:8])([Cl:7])[Cl:1])(=[O:12])[C:10]([CH3:16])=[CH2:15].[Cl:9][C:10]([CH3:16])([CH3:15])[C:11]([O:5][C:3]([CH3:6])([CH3:4])[C:2]([Cl:8])([Cl:7])[Cl:1])=[O:12]参加物
6
実験手順
The analysis of the crude reaction solution by gas chromatography revealed that the conversion of 1,1,1-trichloro-2-methyl-2-propanol was 70.0% and the yield of methyl 2-chloro-2-methylpropanoate was 23.9%. As to other products, it was obtained methyl methacrylate in a 0.7% yield, methacrylic acid in a 0.2% yield, (1,1,1-trichloro-2-methyl-2-propyl) methacrylate in a 7.8% yield, and (1,1,1-trichloro-2-methyl-2-propyl) 2-chloro-2-methylpropanoate in a 12.9% yield.
後処理
- customThe analysis of the crude reaction solution by gas chromatography
出典と根拠
- ORDレコード
- ord-cd5ea02083ee44c7be71b659732e9e78
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09238612B2
関連ノート
読み込み中…