反応式
[CH3:1][C:2]1([CH3:34])[C@@H:4]([CH2:5][C:6](=[N:8][O:9]CC(C)(C)C)[CH3:7])[C@H:3]1[C:15]([O:17][CH:18]([C:32]#[N:33])[C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([O:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:20]=1)=[O:16].[CH3:35][C:36]1(C)[C@@H](CC(=NOCC(C)C)C)[C@H:37]1C(OCC1C=CC=C(OC2C=CC=CC=2)C=1)=O.CC1(C)[C@@H](CC(=NOCC2CC2)C)[C@H]1C(OC(C#N)C1C=CC=C(OC2C=CC=CC=2)C=1)=O.CC1(C)[C@@H](CC(=NOCC2CCC2)C)[C@H]1C(OC(C#N)C1C=CC=C(OC2C=CC=CC=2)C=1)=O.C(C(O)C1C=CC=C(OC2C=CC=CC=2)C=1)#C.C1(=O)N(CO)C(=O)C2CCCCC1=2.ClC1C=CC=C(Cl)C=1CO.CC1C(O)CC(=O)C=1CC=C>>[CH3:34][C:2]1([CH3:1])[C@@H:4]([CH2:5][C:6](=[N:8][O:9][CH:36]([CH3:37])[CH3:35])[CH3:7])[C@H:3]1[C:15]([O:17][CH:18]([C:32]#[N:33])[C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([O:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:20]=1)=[O:16]参加物
9
反応物 8
生成物 1
実験手順
Following procedures similar to Embodiment II above: α-cyano -3-phenoxybenzyl (1R,cis)-2,2-dimethyl-3-(2-(neopentoxyimino)propyl)cyclopropanecarboxylate, 3-phenoxybenzyl (1R,cis)-2,2-dimethyl-3-(2-(isobutoxyimino)propyl)cyclopropanecarboxylate, α-cyano-3-phenoxybenzyl (1R,cis)-2,2-dimethyl-3-(2-(cyclopropylmethoxyimino)propyl)cyclopropanecarboxylate, α-cyano-3-phenoxybenzyl (1R,cis)-2,2-dimethyl-3-(2-(cyclobutylmethoxyimino)propyl)cyclopropanecarboxylate are prepared as well as the corresponding esters in the racemic and (1R,trans) form and similar esters with other alcohols: α-ethynyl-3-phenoxybenzyl alcohol, 3,4,5,6-tetrahydrophthalimidomethyl alcohol, 2,6-dichlorobenzyl alcohol, 2-chloro-4-phenyl-2-butenl-o1 and allethrolone.
出典と根拠
- ORDレコード
- ord-ee2702e9dd3e44b1b8632b1eefac668c
- 出典データセット
- uspto-grants-1980_12
- 特許番号
- US04242521
関連ノート
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