O-Xylene → TK 12997

HRID 1462930

반응식

HRID 1462930 반응식
C([N:4]([CH2:19][CH:20]=[CH2:21])[C:5]1[N:10]=[C:9]([N:11](CC=C)[CH2:12][CH:13]=[CH2:14])[N:8]=[C:7](Cl)[N:6]=1)C=C.[NH:22]([CH:40]1[CH2:45][C:44]([CH3:47])([CH3:46])[NH:43][C:42]([CH3:49])([CH3:48])[CH2:41]1)[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][NH:29][CH:30]1[CH2:35][C:34]([CH3:37])([CH3:36])[NH:33][C:32]([CH3:39])([CH3:38])[CH2:31]1.[OH-].[Na+].C1(C)C(C)=C[CH:55]=[CH:56][CH:57]=1>O>[CH3:46][C:44]1([CH3:47])[CH2:45][CH:40]([N:22]([C:7]2[N:8]=[C:9]([NH:11][CH2:12][CH:13]=[CH2:14])[N:10]=[C:5]([NH:4][CH2:57][CH:56]=[CH2:55])[N:6]=2)[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][N:29]([C:7]2[N:6]=[C:5]([NH:4][CH2:19][CH:20]=[CH2:21])[N:10]=[C:9]([NH:11][CH2:12][CH:13]=[CH2:14])[N:8]=2)[CH:30]2[CH2:35][C:34]([CH3:37])([CH3:36])[NH:33][C:32]([CH3:38])([CH3:39])[CH2:31]2)[CH2:41][C:42]([CH3:49])([CH3:48])[NH:43]1

참가 물질

6

실험 절차

A mixture of 2,4-bis(diallylamino)-6-chloro-1,3,5-triazine (14.2 grams; 0.046 mole), 4,4'-(hexamethylenediimino)bis(2,2,6,6-tetramethylpiperidine) (9.2 grams; 0.023 mole), powdered sodium hydroxide (1.84 grams; 0.046 mole), and xylene (50 mls) is heated at reflux for 36 hours using a water separator to remove byproduct water. The reaction mixture is then filtered hot and the filtrate is evaporated to obtain a light yellow oil which solidifies on standing. Recrystallization of the solid from hexane gives white needles which on recovery and drying weigh 9.3 grams, mp 119°-120° C.

후처리

  1. temperatureis heated
  2. temperatureat reflux for 36 hours
  3. customto remove byproduct water
  4. filtrationThe reaction mixture is then filtered hot
  5. customthe filtrate is evaporated
  6. customto obtain a light yellow oil which
  7. customRecrystallization of the solid from hexane
  8. customgives white needles which on recovery
  9. customdrying

출처 및 근거

ORD 기록
ord-aebfe3aad0504efe8efca6e9b3cde66d
출처 데이터셋
uspto-grants-1984_07
특허 번호
US04461861

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