Triethyl phosphonoacetate → (E)-ethyl 3-(4-(1-(4-(trifluoromethoxy)phenyl)-1 H-1,2,4-triazol-3-yl)phenyl)acrylate

HRID 573819

反応式

HRID 573819 の反応式
[H-].[Na+].C(OP([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])(OCC)=O)C.[F:17][C:18]([F:40])([F:39])[O:19][C:20]1[CH:25]=[CH:24][C:23]([N:26]2[CH:30]=[N:29][C:28]([C:31]3[CH:38]=[CH:37][C:34]([CH:35]=O)=[CH:33][CH:32]=3)=[N:27]2)=[CH:22][CH:21]=1>O1CCCC1.O>[F:40][C:18]([F:17])([F:39])[O:19][C:20]1[CH:25]=[CH:24][C:23]([N:26]2[CH:30]=[N:29][C:28]([C:31]3[CH:38]=[CH:37][C:34](/[CH:35]=[CH:11]/[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:33][CH:32]=3)=[N:27]2)=[CH:22][CH:21]=1

参加物

6

反応物 3

HCID 13345Triethyl phosphonoacetateHCID 24758Sodium hydrideHCID 578244624-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzaldehyde

生成物 1

HCID 90438191(E)-ethyl 3-(4-(1-(4-(trifluoromethoxy)phenyl)-1 H-1,2,4-triazol-3-yl)phenyl)acrylate収率 101.5%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To an oven-dried 2 L three-necked round bottomed flask equipped with a stirring bar was added sodium hydride (60% oil immersion, 7.20 g, 180 mmol) as a solid that was pre-weighed into a 25-mL vial. This was diluted with anhydrous tetrahydrofuran (1 L) under nitrogen, and the solution was stirred in an ice bath. Ethyl 2-(diethoxyphosphoryl)acetate (30.0 mL, 151 mmol) was added dropwise in portions over 20 minutes, and the reaction was stirred at 0° C. for an additional 2 hours. 4-(1-(4-(Trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzaldehyde (50.0. g, 150 mmol) was added in solid portions over 20 minutes, and the reaction turned orange. After stirring for 30 minutes, the ice bath was removed and the reaction was warmed to room temperature over 1 hour. The reaction was quenched with slow addition of saturated aqueous ammonium chloride (500 mL) and allowed to stand at room temperature overnight. The biphasic reaction mixture was diluted with water and extracted with 1:1 ethyl acetate/hexanes (3×). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated to afford the title compound as an orange solid (61.4 g, 100%): mp 135-137° C.; 1H NMR (400 MHz, CDCl3) δ 8.59 (s, 1H), 8.22 (d, J=8.4 Hz, 2H), 7.85-7.77 (m, 2H), 7.73 (d, J=16.0 Hz, 1H), 7.64 (d, J=8.3 Hz, 2H), 7.40 (d, J=8.3 Hz, 2H), 6.51 (d, J=16.0 Hz, 1H), 4.29 (q, J=7.1 Hz, 2H), 1.35 (t, J=7.1 Hz, 3H); 19F NMR (376 MHz, CDCl3) δ −58.02; ESIMS m/z 404 ([M+H]+).

後処理

  1. customTo an oven-dried 2 L three-necked round bottomed flask equipped with a stirring bar
  2. stirringthe reaction was stirred at 0° C. for an additional 2 hours
  3. stirringAfter stirring for 30 minutes
  4. customthe ice bath was removed
  5. customThe reaction was quenched with slow addition of saturated aqueous ammonium chloride (500 mL)
  6. customThe biphasic reaction mixture
  7. extractionextracted with 1:1 ethyl acetate/hexanes (3×)
  8. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-11a4d240210140d2ada0dc48129fd47c
出典データセット
uspto-grants-2015_05
特許番号
US09029560B2

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