1-Naphthol → N-(4-Ethoxyphenyl)naphthalen-1-amine

HRID 1833951ノート

反応式

HRID 1833951 の反応式
[C:1]1(O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH3:12][CH2:13][O:14][C:15]1[CH:16]=[CH:17][C:18]([NH2:21])=[CH:19][CH:20]=1.P(OC1C=CC=CC=1)(OC1C=CC=CC=1)OC1C=CC=CC=1>O>[CH2:13]([O:14][C:15]1[CH:16]=[CH:17][C:18]([NH:21][C:1]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH:4]=[CH:3][CH:2]=2)=[CH:19][CH:20]=1)[CH3:12]

参加物

5

反応物 3

HCID 70051-NaphtholHCID 7540Triphenyl phosphiteHCID 90764-Ethoxyaniline

生成物 1

HCID 80716N-(4-Ethoxyphenyl)naphthalen-1-amine収率 97%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
220 °C

実験手順

288 parts of α-naphthol, 411 parts of p-phenetidine and 10 parts of triphenyl phosphite are mixed and heated to 220° C. At this temperature, the elimination of water commences. In the course of 8 hours, the reaction temperature rises to 250° C, at which stage the reaction has ended. 36 parts of water are removed. After removing excess p-phenetidine, N-p-ethoxy-phenyl-α-naphthylamine distils at a boiling point of 233° - 235° C/5 mm Hg. 510 parts of end product of melting point 73° - 75° C are obtained. This corresponds to a yield of 97% of theory.

後処理

  1. customIn the course of 8 hours
  2. customrises to 250° C, at which stage
  3. custom36 parts of water are removed
  4. customAfter removing excess p-phenetidine, N-p-ethoxy-phenyl-α-naphthylamine
  5. customdistils at a boiling point of 233° - 235° C/5 mm Hg
  6. custom510 parts of end product of melting point 73° - 75° C are obtained

出典と根拠

ORDレコード
ord-5534a28717a94f0b91cc7c5b0810d8fb
出典データセット
uspto-grants-1978_01
特許番号
US04067903

反応ノート

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