反応式
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([CH2:12][OH:13])=[CH:4][CH:3]=1.C1C=C[NH+]=CC=1.[O-][Cr](Cl)(=O)=O.[Si](=O)=O>ClCCl>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([CH:12]=[O:13])=[CH:4][CH:3]=1参加物
5
実験手順
Into a 250-mL round-bottom flask, was placed dichloromethane (150 mL), (4-bromonaphthalen-1-yl)methanol (6.3 g, 26.57 mmol, 1.00 equiv), PCC (11.4 g, 183.72 mmol, 2.00 equiv) and 20 g Silicon dioxide. The resulting solution was stirred for 2 h at room temperature. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column and washed with ethyl acetate/petroleum ether (1/10-1/5). This resulted in 5.3 g (85%) of 4-bromonaphthalene-1-carbaldehyde as a white solid.
後処理
- customInto a 250-mL round-bottom flask, was placed
- concentrationThe resulting mixture was concentrated under vacuum
- washwashed with ethyl acetate/petroleum ether (1/10-1/5)
- customThis resulted in 5.3 g (85%) of 4-bromonaphthalene-1-carbaldehyde as a white solid
出典と根拠
- ORDレコード
- ord-23f9c1c5053945dbbc1c89cd994089ef
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447084B2
関連ノート
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