反応式
O[CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=[O:11].C([CH2:14][C:15]([OH:17])=[O:16])#N>>[OH:11][CH:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[C:10]([CH2:14][C:15]([OH:17])=[O:16])=[CH:2]1参加物
3
実験手順
In an alternative preparation scheme, the intermediate hydroxy-indanone can be reacted with cyanoacetic acid to give the corresponding hydroxyindene-3-acetic acid, which is then esterified before introduction of the R5 -methylene grouping in order to facilitate the purification of desired intermediates. Since introduction of the R5 -methylene grouping is accompanied by ester hydrolysis, the intermediate free acid is re-esterified to facilitate purification followed by reaction with an appropriate halo-alkyl-A group to yield the desired final product ##STR15## can be prepared by reacting a halo-indene-3-acetic acid with a A(CH2)n -containing benzaldehyde prepared from the corresponding individual components ##STR16##
後処理
- customIn an alternative preparation scheme
出典と根拠
- ORDレコード
- ord-d0ba388856fa4b2b9d439c453becd9a4
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05420289
関連ノート
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