反応式
[Br:1]Br.[OH:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH:10]=[C:9]([CH:14]=[O:15])[CH:8]=[CH:7]2.O>C(O)(=O)C>[Br:1][C:5]1[C:4]([OH:3])=[CH:13][CH:12]=[C:11]2[C:6]=1[CH:7]=[CH:8][C:9]([CH:14]=[O:15])=[CH:10]2参加物
5
実験手順
Step b) Bromine (7.45 mL, 145.3 mmol) was added dropwise to a cold (0° C.) solution of 6-hydroxy-2-naphthaldehyde (25.0 g, 145.3 mmol) in acetic acid (300 mL). After stirring for 30 minutes the mixture was poured into water (21), and the precipitated solid filtered and dried to yield a brown solid (34.5 g, 94% yield, m.p. 189-190).
後処理
- filtrationthe precipitated solid filtered
- customdried
- customto yield a brown solid (34.5 g, 94% yield, m.p. 189-190)
出典と根拠
- ORDレコード
- ord-e3c8938ecf0449b9b05442428f6fd33f
- 出典データセット
- uspto-grants-1996_01
- 特許番号
- US05482968
関連ノート
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