反応式
C1OC1C.[CH2:5]1[O:7][CH2:6]1.C(OC)=C.[CH3:12][O:13][CH:14]([O:21][CH3:22])[CH2:15][CH:16]([O:19][CH3:20])[O:17][CH3:18].COC(OC)CC1OCCO1.COC(OC(OC)CC(OC)OC)C>C(OC)=O>[CH3:22][O:21][CH:14]([O:13][CH2:12][CH2:6][O:7][CH3:5])[CH2:15][CH:16]1[O:19][CH2:20][CH2:18][O:17]1参加物
8
反応物 6
生成物 1
試薬・触媒・溶媒 1
実験手順
The procedure described in Example 4 is followed, but instead of the propylene oxide solution 107 parts by volume/hour of a 50 percent strength by weight solution of ethylene oxide in methyl formate are used. In this example, only 40 parts by volume/hour of the methyl vinyl ether solution are employed. After working up as in Example 4, a mixture of 1,1,3,3-tetramethoxypropane, 2-(2',2'-dimethoxyethyl)-(1,3)-dioxolane, malondialdehyde bis-(ethyleneacetal), 1-methoxyethoxy-1,3,3-trimethoxypropane and 2-(2'-methoxy-2'-methoxyethoxy-ethyl)-(1,3)-dioxolane is obtained as the end product, the composition being as in Example 2.
出典と根拠
- ORDレコード
- ord-c21d9f2965cf4dc7b5c827d9ae82703b
- 出典データセット
- uspto-grants-1985_05
- 特許番号
- US04518785
関連ノート
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