反応式
[C:1]1([C:7]2[N:8]=[CH:9][O:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[N+:12]([C:4]1[CH:3]=[CH:2][C:1]([C:7]2[N:8]=[CH:9][O:10][CH:11]=2)=[CH:6][CH:5]=1)([O-:14])=[O:13]参加物
4
実験手順
4-Phenyloxazole (1 g, 6.89 mmol) was dissolved in concentrated sulfuric acid (5 mL) at 0° C. A cold solution of nitrating mixture (prepared by adding 3 mL conc. nitric acid to 5 mL of ice-cold conc. sulfuric acid) was added over 10 minutes. The mixture was allowed to warm to r.t. and stirred for 1 h. The resulting solution was poured into ice-cold water giving a white precipitate, which was filtered and washed thoroughly with water. The solid was dissolved in DCM and washed with water then brine. The organic phase was dried over sodium sulfate and concentrated to yield 4-(4-nitro-phenyl)-oxazole (550 mg, 42%) as a white solid.
後処理
- additionwas added over 10 minutes
- additionThe resulting solution was poured into ice-cold water giving a white precipitate, which
- filtrationwas filtered
- washwashed thoroughly with water
- dissolutionThe solid was dissolved in DCM
- washwashed with water
- dry with materialThe organic phase was dried over sodium sulfate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-ffd008174f1c460f823e039a0141c6bd
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08604029B2
関連ノート
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