Toluene → Ethyl 4-chloro-8-(trifluoromethyl)quinoline-3-carboxylate

HRID 2104474

반응식

HRID 2104474 반응식
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1O)=[CH:13][CH:12]=[CH:11][C:10]=2[C:17]([F:20])([F:19])[F:18])=[O:5])[CH3:2].C1(C)C=CC=CC=1.O=P(Cl)(Cl)[Cl:30].C([O-])(O)=O.[Na+]>C(OCC)(=O)C>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[Cl:30])=[CH:13][CH:12]=[CH:11][C:10]=2[C:17]([F:20])([F:19])[F:18])=[O:5])[CH3:2]

참가 물질

6

반응물 4

HCID 1140TolueneHCID 24813Phosphorus oxychlorideHCID 516892Sodium BicarbonateHCID 178469613HCID 178469613, 화합물

생성물 1

HCID 725465Ethyl 4-chloro-8-(trifluoromethyl)quinoline-3-carboxylate

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

4-Hydroxy-8-(trifluoromethyl)-3-quinolinecarboxylic acid ethyl ester (compound of formula (V)), 11.27 g, 39.55 mmol) was taken into toluene (125 mL), then POCl3 (7.4 mL, 79.08 mmol) was added and the mixture was refluxed for 1.5 hours. The reaction was carefully poured into ice-water with vigorous stirring, then added carefully added saturated NaHCO3 until the solution was neutral. Dilute with ethyl acetate and separate the layers. The organic layer was dried over MgSO4, filtered and concentrated. The resulting material was passed through a short silica gel plug using 10% ethyl acetate in hexane. Concentration and drying under high vacuum yielded 9.93 g of the title compound as a white solid.

후처리

  1. temperaturethe mixture was refluxed for 1.5 hours
  2. customseparate the layers
  3. dry with materialThe organic layer was dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. concentrationConcentration
  7. customdrying under high vacuum

출처 및 근거

ORD 기록
ord-c5a3fd7dce1d4682a2bb4285cef7041c
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07576215B2

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