反応式
[CH:1](/[N:4]1[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[C:10]2[C:5]1=[CH:6][CH:7]=[CH:8][CH:9]=2)=[CH:2]\[CH3:3].CO>ClCCl>[CH:1]([N:4]1[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[C:10]2[C:5]1=[CH:6][CH:7]=[CH:8][CH:9]=2)=[CH:2][CH3:3]参加物
4
実験手順
In a vial, 0.5 g of trans-9-(1-propenyl)carbazole and 0.013 g of IOC10 (2 mole % based on 9-(1-propenyl)carbazole) were dissolved in 1 mL of dichloromethane. The solution was exposed to UV light using a GE H3T-7 200 W medium pressure mercury arc lamp for 3 minutes and then poured into methanol. After filtering and drying the resulting precipitated oligomer in a vacuum oven, a yield of 0.25 g (50%) was obtained.
後処理
- customfor 3 minutes
- filtrationAfter filtering
- customdrying the resulting
- customprecipitated oligomer in a vacuum oven
- customa yield of 0.25 g (50%) was obtained
出典と根拠
- ORDレコード
- ord-4b4b1bebdd3241a29a8e2aa95a8a5480
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06593388B2
関連ノート
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