Trimethylamine → (5-Phenyl-2-benzoxazolinylidene)malononitrile

HRID 436691

反応式

HRID 436691 の反応式
[NH2:1][C:2]1C=CC=[CH:4][C:3]=1O.[NH2:9][C:10]1[CH:15]=[C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:13]=[CH:12][C:11]=1[OH:22].C[N:24]([CH3:26])C>C(O)C>[C:16]1([C:14]2[CH:13]=[CH:12][C:11]3[O:22][C:4](=[C:3]([C:26]#[N:24])[C:2]#[N:1])[NH:9][C:10]=3[CH:15]=2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

5

反応物 3

HCID 1146TrimethylamineHCID 58012-AminophenolHCID 145622-Amino-4-phenylphenol

生成物 1

HCID 20320246(5-Phenyl-2-benzoxazolinylidene)malononitrile

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

The procedure described in Example 1 is repeated using, instead of 2-aminophenol, an equivalent amount of 2-amino-4-phenylphenol in ethanol and holding the mixture under reflux in the presence of 1 ml. of trimethylamine for 60 hours. The crude product is crystallized from acetone to obtain (5-phenyl-2-benzoxazolinylidene)malononitrile of melting point ca. 236° C. (dec.).

後処理

  1. temperatureunder reflux in the presence of 1 ml
  2. customThe crude product is crystallized from acetone

出典と根拠

ORDレコード
ord-1a2c7917b17443e9ad161ac82e76afd4
出典データセット
uspto-grants-1977_06
特許番号
US04028089

関連ノート

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