M-Cresol → 2-(2-Hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine

HRID 23851

반응식

HRID 23851 반응식
Cl[C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([O:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:10][CH:9]=2)[N:5]=[C:4]([C:21]2[CH:26]=[CH:25][C:24]([O:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)=[CH:23][CH:22]=2)[N:3]=1.[CH:34]1[C:39]([OH:40])=[CH:38][CH:37]=[CH:36][C:35]=1[CH3:41].[Al+3].[Cl-].[Cl-].[Cl-].N1C=CC=NN=1>ClC1C=CC=CC=1>[OH:40][C:39]1[CH:34]=[C:35]([CH3:41])[CH:36]=[CH:37][C:38]=1[C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([O:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:10][CH:9]=2)[N:5]=[C:4]([C:21]2[CH:26]=[CH:25][C:24]([O:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)=[CH:23][CH:22]=2)[N:3]=1

참가 물질

6

반응 조건

온도
70 °C

실험 절차

A mixture of 0.9 gm of 2-chloro-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine, 0.24 gm of m-cresol and 0.4 gm AlCl3 in 5 ml chlorobenzene was heated to 70° C. under nitrogen and efficient stirring. After about 4 hr at 70° C., the reaction mixture was analyzed by HPLC, which showed the formation of a new product, and almost disappearance of the starting triazine. The reaction mixture was cooled to room temperature and quenched with water. It was then extracted with methylene chloride, and the organic layer separated, washed with water, dried, and concentrated to give a crude product. The crude product was crystallized from acetone to give almost pure 2-(2-hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine identified by HPLC, NMR and mass spectroscopy.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customquenched with water
  3. extractionIt was then extracted with methylene chloride
  4. customthe organic layer separated
  5. washwashed with water
  6. customdried
  7. concentrationconcentrated
  8. customto give a crude product
  9. customThe crude product was crystallized from acetone

출처 및 근거

ORD 기록
ord-3c8ad07ec9e243c7b04ad3605668233c
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06855269B2

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