Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → (Z)-5,5-bis(2-fluorophenyl)-2,4-pentadienoic acid ethyl ester
反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[F:18])=[CH:9][CH:10]=O.[C:19]([CH:24]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:21][CH2:22][CH3:23])=[O:20]>CO>[CH2:22]([O:21][C:19](=[O:20])/[CH:24]=[CH:10]\[CH:9]=[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[F:18])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[F:1])[CH3:23].[CH2:22]([O:21][C:19](=[O:20])/[CH:24]=[CH:10]/[CH:9]=[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[F:18])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[F:1])[CH3:23]参加物
5
反応物 2
生成物 2
試薬・触媒・溶媒 1
実験手順
As described in Example 99, 3,3-bis(2-fluorophenyl)-2-propenal (1.85 g) was reacted with (carbethoxymethylene)triphenylphosphine (2.8 g) in methanol. The mixture of esters obtained from the usual work up was separated by HPLC (dichloro- methane-hexane; 1:2) to yield 0.4 g of (Z)-5,5-bis(2-fluoro- phenyl)-2,4-pentadienoic acid ethyl ester as an oil and 1.7 g of (E)-5,5-bis(2-fluorophenyl)-2,4-pentadienoic acid ethyl ester as an oil.
後処理
- customobtained from the usual work
- customup was separated by HPLC (dichloro- methane-hexane; 1:2)
出典と根拠
- ORDレコード
- ord-acbfd5066b52431892df870721b0ce39
- 出典データセット
- uspto-grants-1990_12
- 特許番号
- US04975438
反応ノート
読み込み中…