Toluene → 2-Methoxymethyl-2-methyl-6-cyano-4-chromanone
反応式
[C:1]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][C:11]=1[OH:12])[C:7]#[N:8])(=[O:3])[CH3:2].[CH3:13][O:14][CH2:15][C:16](=O)[CH3:17].N1CCCC1.C1(C)C=CC=CC=1>O>[CH3:13][O:14][CH2:15][C:16]1([CH3:17])[CH2:2][C:1](=[O:3])[C:4]2[C:11](=[CH:10][CH:9]=[C:6]([C:7]#[N:8])[CH:5]=2)[O:12]1参加物
6
実験手順
a mixture of 50 g of 3-acetyl-4-hydroxybenzonitrile, 70 ml of methoxy-2-propanone, 6 ml of pyrrolidine and 300 ml of toluene is boiled in a water separator for 3 hours. The mixture is evaporated, the residue is worked up in the customary manner (ethyl acetate/dil. hydrochloric acid) and 2-methoxymethyl-2-methyl-6-cyano-4-chromanone is obtained, m.p. 79°-81° C.
後処理
- customThe mixture is evaporated
出典と根拠
- ORDレコード
- ord-9562ccf88c7f43e1bc049adc16efce4c
- 出典データセット
- uspto-grants-1992_07
- 特許番号
- US05130322
反応ノート
読み込み中…