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Malonic Acid → 2,4,8-Trichloro-7-methoxyquinoline

HRID 530724
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HRID 530724 반응식
[ClH:1].[Cl:2][C:3]1[C:9]([O:10][CH3:11])=[CH:8][CH:7]=[CH:6][C:4]=1[NH2:5].[C:12](O)(=O)[CH2:13][C:14](O)=O.O(Cl)[Cl:20].[P]>O>[Cl:1][C:14]1[CH:13]=[C:12]([Cl:20])[C:6]2[C:4](=[C:3]([Cl:2])[C:9]([O:10][CH3:11])=[CH:8][CH:7]=2)[N:5]=1
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참가 물질

5

반응물 3

HCID 867Malonic AcidHCID 248201302-Chloro-3-methoxyaniline hydrochlorideHCID 178479709HCID 178479709, 화합물

생성물 1

HCID 27945162,4,8-Trichloro-7-methoxyquinoline수율 74%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 2-chloro-3-methoxyaniline hydrochloride 215d (15 g, 1 eq.), malonic acid (12.06 g, 1.5 eq.), and phosphorus oxochloride (80 mL) was refluxed for 16 hrs. The reaction mixture was slowly poured into water and extracted with DCM. The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material was purified on silica pad, eluted with DCM, to yield compound 220d as a white solid in 74% yield. 1H NMR (CDCl3, 376 MHz) δ 4.10 (s, 3H), 7.43 (t, J=4.88 Hz, 2H), 8.12 (d, J=9.48 Hz, 1H).

후처리

  1. temperaturewas refluxed for 16 hrs
  2. extractionextracted with DCM
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe crude material was purified on silica pad
  7. washeluted with DCM

출처 및 근거

ORD 기록
ord-35aff3fb39fa404e9872d6cead9f8f2f
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353100B2

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