Triethyl phosphonoacetate → HCID 90438191, 화합물

HRID 573819

반응식

HRID 573819 반응식
[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

참가 물질

6

반응물 3

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

생성물 1

HCID 90438191HCID 90438191, 화합물수율 101.5%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

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]+).

후처리

  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

출처 및 근거

ORD 기록
ord-11a4d240210140d2ada0dc48129fd47c
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09029560B2

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