反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:17][CH:16]([C:18]([OH:20])=[O:19])[CH2:15][C:8]3([C:12](=[O:13])[NH:11][C:10](=[O:14])[NH:9]3)[C:6]=2[CH:7]=1.[CH2:21](O)[CH2:22][O:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][CH2:30][CH2:31][O:32][CH3:33].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH2:21]([O:19][C:18]([CH:16]1[CH2:15][C:8]2([C:12](=[O:13])[NH:11][C:10](=[O:14])[NH:9]2)[C:6]2[CH:7]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=2[O:17]1)=[O:20])[CH2:22][O:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][CH2:30][CH2:31][O:32][CH3:33]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture consisting of 6-fluoro-2,3-dihydro-2',5'-dioxo-spiro[4H-1-benzopyran-4,4'-imidazolidine]-2-carboxylic acid (2.8 g, 0.01 mol) (obtained through the process as described in Example 1), 3,6,9,12-tetraoxatridecanol (2.1 g, 0.01 mol) and p-toluenesulfonic acid (1.9 g, 0.01 mol) in 80 ml of toluene was heated at reflux temperature for 7.0 hours under a Dean-Stark trap. The reaction mixture was evaporated in vacuo to give a semi-solid residue which was partitioned between 50 ml of chloroform and 50 ml of water. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to give a pale yellow oil which was chromatographed on silica gel, eluting with ethyl acetate to give 3.9 g (82.5%) of the desired refined compound as a colorless oil.
後処理
- customobtained through the process
- temperaturewas heated
- temperatureat reflux temperature for 7.0 hours under a Dean-Stark trap
- customThe reaction mixture was evaporated in vacuo
- customto give a semi-solid residue which
- customwas partitioned between 50 ml of chloroform and 50 ml of water
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationfiltered
- customevaporated in vacuo
- customto give a pale yellow oil which
- customwas chromatographed on silica gel
- washeluting with ethyl acetate
出典と根拠
- ORDレコード
- ord-77d69230e80e423a957f0968193c264e
- 出典データセット
- uspto-grants-1988_04
- 特許番号
- US04740517
関連ノート
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