反応式
C([O:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[N:7]=1)(=O)C.[ClH:13]>>[ClH:13].[CH3:12][C:8]1[N:7]=[C:6]([CH2:5][OH:4])[CH:11]=[CH:10][CH:9]=1参加物
3
実験手順
A solution of (6-methylpyridin-2-yl)methyl acetate (1.0 g) in concentrated HCl (3 mL) was refluxed for 1 h. The reaction mixture was then concentrated in vacuo to obtain the crude product. The crude material was azeotroped with toluene, and the residue obtained was filtered and dried in vacuo to afford (6-methylpyridin-2-yl)methanol hydrochloride (811 mg) as a solid.
後処理
- concentrationThe reaction mixture was then concentrated in vacuo
- customto obtain the crude product
- customThe crude material was azeotroped with toluene
- customthe residue obtained
- filtrationwas filtered
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-fbf72e3296044ccb8ffa6a04d73dd71d
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08481534B2
関連ノート
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