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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Aniline → Formanilide

HRID 1390853
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HRID 1390853 반응식
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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6115AnilineHCID 86736349Potassium formanilide

생성물 1

HCID 7671Formanilide

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
100 °C

실험 절차

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%.

후처리

  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

출처 및 근거

ORD 기록
ord-6963e4ec0ac247f39f78bdd4c60ac559
출처 데이터셋
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04140716

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