Acetone → HCID 178481590、化合物
反応式
[CH3:1][C:2]([C:5]1[O:9][N:8]=[C:7]([N:10]2[CH:14]([OH:15])[CH:13]([OH:16])[N:12]([CH3:17])[C:11]2=[O:18])[CH:6]=1)([CH3:4])[CH3:3].CC(C)=O>Cl(O)(=O)(=O)=O.O>[CH2-:2][C:5]([CH3:6])=[O:9].[CH3:4][C:2]([C:5]1[O:9][N:8]=[C:7]([N:10]2[CH:14]([OH:15])[CH:13]([OH:16])[N:12]([CH3:17])[C:11]2=[O:18])[CH:6]=1)([CH3:1])[CH3:3]参加物
5
実験手順
To a solution of 1.0 gram of 3-[5-(1,1-dimethylethyl)-3-isoxazolyl]-4,5-dihydroxy-1-methyl-2-imidazolidinone in 20 ml. of anhydrous acetone were added three drops of 70% perchloric acid. The reaction mixture stood at ambient temperature for sixteen hours, and then was diluted with 100 ml. of water. The white crystalline precipitate was collected by filtration and recrystallized from diethyl ether and hexane to afford 3-[5-(1,1-dimethylethyl)-3-isoxazolyl]4,5-dihydroxy-1-methyl-2-imidazolidinone acetonide. M.P. 157°-159° C. Mass Spectrum M+Theory 295; Found 295.
後処理
- waitThe reaction mixture stood at ambient temperature for sixteen hours
- additionwas diluted with 100 ml
- filtrationThe white crystalline precipitate was collected by filtration
- customrecrystallized from diethyl ether and hexane
出典と根拠
- ORDレコード
- ord-2b8986e1e1d94d508231d76940c60c38
- 出典データセット
- uspto-grants-1982_10
- 特許番号
- US04354030
反応ノート
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