反応式
[CH3:1][O:2][C:3](=[O:13])[CH2:4][CH2:5][CH2:6][CH2:7][CH:8](OC)[O:9]C.Cl>CO>[C:3]([CH2:4][CH2:5][CH2:6][CH2:7][CH:8]=[O:9])([O:2][CH3:1])=[O:13]参加物
4
実験手順
After the reaction, MeOH was recovered, following by the same treatment as above to give 9.47 g. of crude 6,6-dimethoxycaproic acid methyl ester. Then, a 10 wt.% aqueous hydrochloric acid solution was added to this crude product, followed by stirring for 6 hours at room temperature. The reaction mixture was treated by usual method to give crude products. Pure 3.20 g. of 5-carbomethoxy-1-pentanal was obtained by column chromatography.
後処理
- customwas recovered
- customto give 9.47 g
- additionThe reaction mixture was treated by usual method
- customto give crude products
出典と根拠
- ORDレコード
- ord-18e99ebb93034446a33f27fb49e9b384
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04609492
関連ノート
読み込み中…