反応式
C[O:2]N=C1C2C(=CC=C(C(O)=O)C=2C)SCC1.[CH3:18][O:19][N:20]=[C:21]1[C:30]2[C:25](=[C:26](C)[CH:27]=[C:28]([C:32](C3C=NN(CC)C=3OS(CCC)(=O)=O)=[O:33])[C:29]=2[CH3:31])[S:24](=[O:50])(=[O:49])[CH2:23][CH2:22]1.OO.C(OCC)(=O)C>C(O)(=O)C>[CH3:18][O:19][N:20]=[C:21]1[C:30]2[C:25](=[CH:26][CH:27]=[C:28]([C:32]([OH:33])=[O:2])[C:29]=2[CH3:31])[S:24](=[O:50])(=[O:49])[CH2:23][CH2:22]1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
1.0 Gram (4.0 mmol) of the 4-methoxyimino-5-methylthiochroman-6-carboxylic acid obtained in the above (2) was reacted with 1.3 g (12 mmol) of a 30% hydrogen peroxide aqueous solution in 5 ml of acetic acid at 100° C. for 1 hour. Ethyl acetate was added to the reaction product, and the mixture was washed with a saturated sodium chloride aqueous solution and then dried over sodium sulfate. The solvent was distilled off to give 1.1 g (yield 97%) of 4-methoxyimino-5-methylthiochroman-6-carboxylic acid-1,1-dioxide.
後処理
- washthe mixture was washed with a saturated sodium chloride aqueous solution
- dry with materialdried over sodium sulfate
- distillationThe solvent was distilled off
出典と根拠
- ORDレコード
- ord-8c6cd4df0e944072bdac1909224c6ce9
- 出典データセット
- uspto-grants-1998_12
- 特許番号
- US05849926
関連ノート
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