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Formaldehyde → Phenol-Formaldehyde Aniline

HRID 1701770
ノート
印刷プレビュー

反応式

HRID 1701770 の反応式
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C=O>O>[CH2:1]=[O:7].[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 712Formaldehyde2 回HCID 996PhenolHCID 6115Aniline

生成物 1

HCID 168216Phenol-Formaldehyde Aniline

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
90 °C

実験手順

A reactor is charged with a 50:50 wt. percent mixture of phenol and aniline at 50° C. and 15 psig nitrogen. The reactor is heated to 90° C. Formaldehyde is fed into the reactor in an amount of about 10 wt. percent of the phenolaldehyde mixture, while the reactor temperature is maintained at 90° C. After the formaldehyde has been fed into the reactor, the pressure is reduced to zero psig and the mixture is heated to 180° C. and held at that temperature for one hour, during which time a distillate of water of condensation is removed. The mixture is then maintained at 180° C. and 15 mm Hg for 6 hours, during which time a distillate of unreacted phenol and aniline is removed. The yield of PFAR product in the reactor is about 52 wt % of the initial reaction mixture.

後処理

  1. additionA reactor is charged with a 50
  2. temperatureis maintained at 90° C
  3. temperaturethe mixture is heated to 180° C.
  4. customis removed
  5. temperatureThe mixture is then maintained at 180° C.
  6. wait15 mm Hg for 6 hours
  7. customduring which time a distillate of unreacted phenol and aniline is removed
  8. customreaction mixture

出典と根拠

ORDレコード
ord-f3c0b3fa219546feb06d02c0742521e6
出典データセット
uspto-grants-1980_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04195151

反応ノート

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