Hexanoic acid, 4,6,6,6-tetrachloro-3,3-dimethyl-, ethyl ester → 2(3H)-Furanone, 5-(2,2-dichloroethenyl)dihydro-4,4-dimethyl-
反応式
[CH3:1][C:2]([CH3:16])([CH:9](Br)[CH2:10][C:11](Cl)([Cl:13])[Cl:12])[CH2:3][C:4]([O:6]CC)=[O:5].CC(C)(C(Cl)CC(Cl)(Cl)Cl)CC(OCC)=O>>[CH3:1][C:2]1([CH3:16])[CH:9]([CH:10]=[C:11]([Cl:13])[Cl:12])[O:6][C:4](=[O:5])[CH2:3]1参加物
3
実験手順
The procedure of Reference Example 1 was repeated except that 35.4 parts of ethyl 3,3-dimethyl-4-bromo-6,6,6-trichlorohexanoate was used in lieu of ethyl 3,3-dimethyl-4,6,6,6-tetrachlorohexanoate. By this procedure was obtained 19.0 parts of 3,3-dimethyl-4-(2',2'-dichlorovinyl)-4-butanolide (yield 90%).
出典と根拠
- ORDレコード
- ord-bd5e46d01c7841208a14c90b6c6d502e
- 出典データセット
- uspto-grants-1984_07
- 特許番号
- US04458090
反応ノート
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