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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Aniline → Formanilide

HRID 1390853
ノート
印刷プレビュー

反応式

HRID 1390853 の反応式
NC1C=CC=CC=1.[CH:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9].[K]>CO>[CH:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9]
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

4

反応物 2

HCID 6115AnilineHCID 86736349Potassium formanilide

生成物 1

HCID 7671Formanilide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
100 °C

実験手順

Into a 1-liter Parr autoclave equipped with an agitator, thermowell, rupture disc and cooling coils are placed 84 g. (0.9 mole) of aniline, 16 g. (0.1 mole) of potassium formanilide and 150 g. of methanol. The autoclave is closed and purged with CO. The temperature is raised to 100° C. with atm. steam and CO is introduced at 28 kg/cm2 pressure. Absorption is rapid and little or no heat of reaction is noted. The reaction is run for 31/2 hours, the autoclave cooled to 15° C. and the excess CO vented. The methanol is removed by distillation, xylene added and resulting xylene solution washed with 10 ml. of conc. hydrochloric acid and 200 ml. of water. The organic layer is separated and analyzed by gas-liquid chromatography. The yield of formanilide expected is approximately 93%.

後処理

  1. customInto a 1-liter Parr autoclave equipped with an agitator
  2. temperaturethermowell, rupture disc and cooling coils
  3. customThe autoclave is closed
  4. custompurged with CO
  5. additionsteam and CO is introduced at 28 kg/cm2 pressure
  6. customAbsorption
  7. temperaturelittle or no heat of reaction
  8. custom2 hours
  9. temperaturethe autoclave cooled to 15° C.
  10. customThe methanol is removed by distillation, xylene
  11. additionadded
  12. customresulting xylene solution
  13. washwashed with 10 ml
  14. customThe organic layer is separated

出典と根拠

ORDレコード
ord-6963e4ec0ac247f39f78bdd4c60ac559
出典データセット
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04140716

反応ノート

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