O-Xylene → TK 12997

HRID 1462930

反応式

HRID 1462930 の反応式
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

参加物

6

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-aebfe3aad0504efe8efca6e9b3cde66d
出典データセット
uspto-grants-1984_07
特許番号
US04461861

関連ノート

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