反応式
[OH-].[Na+].[OH:3][C:4]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:5]=1[C:11](=[O:15])[CH2:12][CH2:13]Cl.S(=O)(=O)(O)O>>[OH:10][C:8]1[CH:7]=[CH:6][C:5]2[C:11](=[O:15])[CH:12]=[CH:13][O:3][C:4]=2[CH:9]=1参加物
4
実験手順
To a cooled (5° C.) solution of 2N sodium hydroxide (10.0 L) was added the compound of step A (244.1 g) in one portion. The solution was warmed to room temperature over 2 hours using a warm water bath then recooled to 5° C. and the pH adjusted to 2 with 6M sulfuric acid (1.2 L). The mixture was extracted with 3×3.0 L of ethyl acetate, washed with brine (1×2.0 L) dried over sodium sulfate and filtered. Concentration in vacuo gave a tan solid. Trituration with hexanes, and filtration afforded 173.7 g (58% yield) of the title compound. M.P. 136° C.-137° C.
後処理
- customthen recooled to 5° C.
- extractionThe mixture was extracted with 3×3.0 L of ethyl acetate
- washwashed with brine (1×2.0 L)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationConcentration in vacuo
- customgave a tan solid
- filtrationTrituration with hexanes, and filtration
出典と根拠
- ORDレコード
- ord-850973f56ac44474b4b10b2933702cb0
- 出典データセット
- uspto-grants-1996_09
- 特許番号
- US05552435
関連ノート
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