1,1-Bis(propan-2-yl) 3,3-dimethoxycyclobutane-1,1-dicarboxylate → 7-Chloro-2-phenyl4-trifluoromethyl-quinoline

HRID 386298

반응식

HRID 386298 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:10][C:11](=O)[C:12]([F:15])([F:14])[F:13])[CH:5]=[CH:6][CH:7]=1.C(OC(C1(C(OC(C)C)=O)CC(OC)(OC)C1)=O)(C)C>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:5]([C:11]([C:12]([F:15])([F:14])[F:13])=[CH:10][C:9]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[N:8]2)=[CH:6][CH:7]=1

참가 물질

3

실험 절차

4-(3-Chloro-phenylamino)-1,1,1-trifluoro-4-phenyl-but-3-en-2-one (2.8 g, 0.0086 mole) and polyphosphoric acid (60 mL) in a 250 mL 3 neck round bottom flask was stirred mechanically under an atmosphere of Nitrogen at 165° C. internal temperature for 3 h. The reaction was poured over stirring ice water (600 ml). The product precipitated, and was collected by suction filtration, washed with water, and air dried overnight. The solids remaining in the Buchner funnel, and beaker from aqueous quench were rinsed into a flask concentrated in vacuo, then combined with the filtered sample and chromatographed on silica gel with 3:1 Hexanes/methylene chloride to afford the title compound as a white solid; 1H NMR (CDCl3, 400 MHz) δ 7.53-7.59 (m, 3 H), 7.60-7.63 (dd, 1 H, J=2.2 & J=9.1 Hz), 8.06-8.09 (dq, 1 H, J=1.9 & J=9.0 Hz), 8.16-8.20 (m, 3 H), 8.29 (d, 1H, J=2.1 Hz); 19F NMR 5-61.48; MS (ES+): 308.0 (100) [MH+], 310.0 (30) [M+2H+].

후처리

  1. additionThe reaction was poured
  2. customThe product precipitated
  3. filtrationwas collected by suction filtration
  4. washwashed with water, and air
  5. customdried overnight
  6. customfrom aqueous quench
  7. washwere rinsed into a flask
  8. concentrationconcentrated in vacuo
  9. customchromatographed on silica gel with 3:1 Hexanes/methylene chloride

출처 및 근거

ORD 기록
ord-b8a8e560ddf34a118bf8935c565850e4
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08367826B2

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