反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[CH3:10][C:11]1([CH3:19])[O:16][C:15](=[O:17])[CH2:14][C:13](=[O:18])[O:12]1>O>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[C:14]2[C:15](=[O:17])[O:16][C:11]([CH3:19])([CH3:10])[O:12][C:13]2=[O:18])=[CH:4][CH:3]=1参加物
4
反応条件
- 温度
- 75 °C
実験手順
To a 500 mL RB flask fitted with magnetic stirrer was charged with water (160 mL). To the stirred solvent was added 4-hydroxybenzaldehyde (25.0 g, 122.12 mmol) and 2,2-dimethyl-1,3-dioxane-4,6-dione (25.0 g), it was heated at 75° C. for 2 h. The RM was cooled to obtain the solid, filtered and was washed with water, then dried to obtain the product (34.0, yield: 83.74%).
後処理
- customTo a 500 mL RB flask fitted with magnetic stirrer
- temperatureThe RM was cooled
- customto obtain the solid
- filtrationfiltered
- washwas washed with water
- customdried
- customto obtain the product (34.0, yield: 83.74%)
出典と根拠
- ORDレコード
- ord-5f43363cbac149b6ae7eeb3af98e69e6
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09278915B2
関連ノート
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