Toluene → 4-Hydroxy-3-propoxybenzaldehyde
反応式
CC1(C)CO[CH:5]([C:8]2[CH:13]=[CH:12][C:11]([OH:14])=[C:10]([O:15][CH2:16][CH2:17][CH3:18])[CH:9]=2)[O:4]C1.C1(C)C=CC=CC=1>C(O)=O>[OH:14][C:11]1[CH:12]=[CH:13][C:8]([CH:5]=[O:4])=[CH:9][C:10]=1[O:15][CH2:16][CH2:17][CH3:18]参加物
4
実験手順
A mixture of 1.26 g (4.74 mmol) of 4-(5,5-dimethyl-1,3-dioxan-2-yl)-2-propoxyphenol, 20 ml of toluene and 20 ml of formic acid was vigorously stirred for 2 hours at room temperature. Thereafter, the reaction mixture was partitioned between toluene and water and the organic phase was washed several times with water, dried over magnesium sulfate, filtered and evaporated down. Crystallization of the residue from a mixture of 10 ml of diethyl ether and 20 ml of hexane gave 0.78 mg of 4-hydroxy-3-propoxybenzaldehyde.
後処理
- customThereafter, the reaction mixture was partitioned between toluene and water
- washthe organic phase was washed several times with water
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated down
- customCrystallization of the residue
- additionfrom a mixture of 10 ml of diethyl ether and 20 ml of hexane
出典と根拠
- ORDレコード
- ord-22979cd9413c4b5fa6b09df8a67e6f1c
- 出典データセット
- uspto-grants-2003_10
- 特許番号
- US06632909B2
反応ノート
読み込み中…