Aniline → N-[(4-chloro-2-methylphenyl)-methylene]benzeneamine

HRID 354588노트

반응식

HRID 354588 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[C:4]([CH3:10])[CH:3]=1.[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1(C)C=CC=CC=1.CCOCC>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[N:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:4]([CH3:10])[CH:3]=1

참가 물질

5

반응물 2

HCID 6115AnilineHCID 27576584-Chloro-2-methylbenzaldehyde

생성물 1

HCID 13553333N-[(4-chloro-2-methylphenyl)-methylene]benzeneamine수율 77%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 3283Diethyl Ether용매

실험 절차

A mixture of 4-chloro-2-methylbenzaldehyde (3.5 g, 22.6 mmol) and aniline (2.11 g, 22.6 mmol) in toluene (40 ml) was heated at reflux in a Dean-Stark apparatus for 1 hour. The mixture was cooled and evaporated in vacuo to leave an oily residue. The residue was redissolved in ether, washed with 5% sodium bicarbonate solution. The organic phase was separated, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo to afford an oily residue which was purified by distillation via a Kugelrohr apparatus (oven temperature 160° C., 0.5 mm) to provide the title compound (4.0 g, 7.4 mmol, 77%) as a viscous oil; pmr (CDCl3)δ2.5(3H, s), 6.3-7.5(7H,m), 7.95(H, d), 8.6(H,s).

후처리

  1. temperaturewas heated
  2. temperatureat reflux in a Dean-Stark apparatus for 1 hour
  3. temperatureThe mixture was cooled
  4. customevaporated in vacuo
  5. customto leave an oily residue
  6. washwashed with 5% sodium bicarbonate solution
  7. customThe organic phase was separated
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated in vacuo
  11. customto afford an oily residue which
  12. distillationwas purified by distillation via a Kugelrohr apparatus (oven temperature 160° C., 0.5 mm)

출처 및 근거

ORD 기록
ord-37bfeadaa64e48a3b4536a3e202c3f49
출처 데이터셋
uspto-grants-1983_03
특허 번호
US04375475

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