反応式
C(O[C:5]1([CH3:14])[CH:9]=[CH:8][C:7](=[O:10])[CH:6]1[CH2:11][C:12]#[CH:13])(=O)C.S(=O)(=O)(O)[OH:16]>>[OH:16][CH:9]1[CH2:8][C:7](=[O:10])[C:6]([CH2:11][C:12]#[CH:13])=[C:5]1[CH3:14]参加物
3
実験手順
In the same flask as in Example 1, 20% sulfuric acid (10 ml) was charged, and dl-3-acetoxy-2-propargyl-3-methyl-4-cyclopentenone (1.92 g) was dropwise added thereto in 1 hour while keeping the inner temperature at 0° C. After completion of the dropwise addition, the resultant mixture was stirred at the same temperature as above for 3 hours. The reaction mixture was subjected to post-treatment and purification as in Example 1 to give 1.38 g of 4-hydroxy-2-propargyl-3-methyl-2-cyclopentenone. Yield, 91%.
後処理
- additionwas dropwise added
- customat 0° C
- additionAfter completion of the dropwise addition
- custompurification as in Example 1
出典と根拠
- ORDレコード
- ord-5e86856ef5f9491a9c995f985afc21e8
- 出典データセット
- uspto-grants-1986_08
- 特許番号
- US04608442
関連ノート
読み込み中…