HCID 86744189、化合物 → Pirazolac
反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[C:11]([C:13]3[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=3)[C:10]([CH2:20][C:21]([O-:23])=[O:22])=[N:9]2)=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH:12]=[C:11]([C:13]3[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=3)[C:10]([CH2:20][C:21]([OH:23])=[O:22])=[N:9]2)=[CH:6][CH:7]=1参加物
3
試薬・触媒・溶媒 1
実験手順
1,49 Grams of the ester prepared according to (a) are stirred in 30 ml of trifluoroacetic acid, at room temperature. The hydrolysis is followed by TLC; at the end the excess of CF3 --COOH is evaporated in vacuo and the residue is crystallized from acetic acid/ethanol. The title product is identical with a sample prepared according to EP 54812.
後処理
- customat the end the excess of CF3 --COOH is evaporated in vacuo
- customthe residue is crystallized from acetic acid/ethanol
- customprepared
出典と根拠
- ORDレコード
- ord-937afe83f5454494b6f401f826828272
- 出典データセット
- uspto-grants-1990_08
- 特許番号
- US04952702
反応ノート
読み込み中…