反応式
[NH2:1][CH:2]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[CH:8]=1)[CH2:3][C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:20]O>>[CH3:20][O:5][C:4](=[O:6])[CH2:3][CH:2]([NH2:1])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[CH:8]=1参加物
4
実験手順
To a solution of 3-amino-3-(3-nitrophenyl)propanoic acid (20.00 g; 95.15 mmol; 1.00 eq.) in MeOH (300 mL) was added thionyl chloride (50.00 ml; 761.22 mmol; 8.00 eq.) at 0° C. slowly. Then the mixture was warmed to room temperature and stirred overnight. The reaction mixture was evaporated and the crude product was purified by flash chromatography on silica gel (MeOH:DCM=15:85) to obtain 20 g of the title compound. LCMS [225 (M+1)].
後処理
- customThe reaction mixture was evaporated
- customthe crude product was purified by flash chromatography on silica gel (MeOH:DCM=15:85)
出典と根拠
- ORDレコード
- ord-6b53fef7badc4ebfa65aaffdfb208b05
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637532B2
関連ノート
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