反応式
[N:1]1[C:8](Cl)=[N:7][C:5](Cl)=[N:4][C:2]=1Cl.[Cl-].[Al+3].[Cl-].[Cl-].[C:14]1([O:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[C:27]1([CH:34]=[CH:33][CH:32]=[C:30]([OH:31])[CH:29]=1)[OH:28]>ClC1C=CC=CC=1Cl>[OH:28][C:27]1[CH:29]=[C:30]([OH:31])[CH:32]=[CH:33][C:34]=1[C:2]1[N:4]=[C:5]([C:32]2[CH:33]=[CH:34][C:27]([OH:28])=[CH:29][C:30]=2[OH:31])[N:7]=[C:8]([C:24]2[CH:23]=[CH:22][C:21]([O:20][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)=[CH:26][CH:25]=2)[N:1]=1参加物
6
実験手順
To a stirring mixture of 9 gm of cyanuric chloride, 20 gm of aluminum chloride in 50 mL of o-dichlorobenzene was added 8.5 gm of phenyl ether followed by 11 gm of resorcinol. The reaction mixture was first stirred at room temperature and then gradually heated to 110-115° C., and then held for 4 hr at this temperature. The heating was discontinued, and the reaction mixture quenched with water. O-Dichlorobenzene was removed azeotropically from the product mixture, the precipitated material filtered, and washed with water. The crude product was purified by column chromatography to give 2.3 gm of pure 2,4-bis(2,4-dihyroxyphenyl)-6-(4-phenoxyphenyl)-1,3,5-triazine, identified by HPLC, NMR, LC-UV and mass spectroscopy.
後処理
- temperaturegradually heated to 110-115° C.
- customthe reaction mixture quenched with water
- customO-Dichlorobenzene was removed azeotropically from the product mixture
- filtrationthe precipitated material filtered
- washwashed with water
- customThe crude product was purified by column chromatography
出典と根拠
- ORDレコード
- ord-96e90055b36f4eb2b8f7413ef1d79199
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06855269B2
関連ノート
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