反応式
S(Cl)(Cl)=O.[CH:5]1[C:10]([C@@H:11]([NH2:15])[C:12]([OH:14])=[O:13])=[CH:9][CH:8]=[C:7]([OH:16])[CH:6]=1.[CH3:17]O>>[CH3:17][O:13][C:12](=[O:14])[CH:11]([NH2:15])[C:10]1[CH:9]=[CH:8][C:7]([OH:16])=[CH:6][CH:5]=1参加物
4
実験手順
To 50 mL of methanol cooled to 0° C. was dropwise added 3.75 mL of thionyl chloride followed by 5.0 g (0.030 mmol) of D-4-hydroxyphenylglycine. The reaction was heated to reflux for 5 h then stirred overnight at room temperature. The resulting mixture was concentrated in vacuo and the residue was diluted with ether. The resulting solid was collected by filtration and dried in vacuo to provide 5.9 g of amino-(4-hydroxy-phenyl)-acetic acid methyl ester as a white solid. Electrospray Mass Spec 182.2 (M+H)+
後処理
- temperatureThe reaction was heated
- temperatureto reflux for 5 h
- concentrationThe resulting mixture was concentrated in vacuo
- additionthe residue was diluted with ether
- filtrationThe resulting solid was collected by filtration
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-a425b517eafc418392926bb6979aa5d9
- 出典データセット
- uspto-grants-2004_11
- 特許番号
- US06812227B2
関連ノート
読み込み中…