ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

1-Methylimidazole → 4-(1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-yloxy)-4-oxobutanoic acid triethylamine salt

HRID 1886893
ノート
印刷プレビュー

反応式

HRID 1886893 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([C:38]2[CH:43]=[CH:42][C:41]([O:44][CH3:45])=[CH:40][CH:39]=2)([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[O:10][CH2:11][CH2:12][CH:13]([OH:31])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[CH:5][CH:4]=1.[C:46]1(=[O:52])[O:51][C:49](=[O:50])[CH2:48][CH2:47]1.[CH2:53]([N:55]([CH2:58][CH3:59])[CH2:56][CH3:57])[CH3:54].CN1C=CN=C1>C(Cl)Cl>[CH2:53]([N:55]([CH2:58][CH3:59])[CH2:56][CH3:57])[CH3:54].[CH3:45][O:44][C:41]1[CH:40]=[CH:39][C:38]([C:9]([C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[O:10][CH2:11][CH2:12][CH:13]([O:31][C:46](=[O:52])[CH2:47][CH2:48][C:49]([OH:51])=[O:50])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[CH:43][CH:42]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 13901-MethylimidazoleHCID 7922Succinic anhydrideHCID 8471TriethylamineHCID 687487641-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-ol

生成物 1

HCID 687468894-(1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-yloxy)-4-oxobutanoic acid triethylamine salt

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒
2 回

実験手順

1-(bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-ol (6.8 g, 11.0 mmoles), succinic anhydride (1.1 g, 11.0 mmoles), triethylamine (4.6 mL, 33.0 mmoles) and 1-methylimidazole (0.44 mL, 5.5 mmoles) are dissolved in methylene chloride (68 mL). The reaction is stirred at ambient temperature for five days, during which time the solution darkened. The solution is then diluted with methylene chloride (100 mL) and washed twice with ice-cold aqueous citric acid (10% [w/v], 50 mL) and once with saturated aqueous sodium chloride (50 mL). The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and evaporated to a dark resin. The crude product is purified on silica gel (200 mL bed volume) eluting with methylene chloride:triethylamine (95:5 [v/v/v], 500 mL), then methylene chloride:methanol:triethylamine (93:2:5 [v/v/v], 1000 mL). Fractions containing pure product by thin layer chromatography are pooled and evaporated to a resin. The resin is dried well in vacuo. The yield is 2.4 g (30%).

後処理

  1. washwashed twice with ice-cold aqueous citric acid (10% [w/v], 50 mL) and once with saturated aqueous sodium chloride (50 mL)
  2. dry with materialThe methylene chloride solution is dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. customevaporated to a dark resin
  5. customThe crude product is purified on silica gel (200 mL bed volume)
  6. washeluting with methylene chloride:triethylamine (95:5 [v/v/v], 500 mL)
  7. additionFractions containing pure product by thin layer chromatography
  8. customevaporated to a resin
  9. customThe resin is dried well in vacuo

出典と根拠

ORDレコード
ord-ddd8ad3cc9354c3692719c4d2c851518
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501706B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート