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Phosgene → 5-iodo-N-methylisatoic anhydride

HRID 1488684
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HRID 1488684 반응식
[I:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=[O:8])[C:5]([NH:11][CH3:12])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[C:19](Cl)(Cl)=[O:20]>O>[I:1][C:2]1[CH:10]=[C:6]2[C:7]([O:9][C:19](=[O:20])[N:11]([CH3:12])[C:5]2=[CH:4][CH:3]=1)=[O:8]
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참가 물질

5

반응물 3

HCID 6371PhosgeneHCID 11430Potassium CarbonateHCID 222818675-Iodo-2-(methylamino)benzoic acid

생성물 1

HCID 538260965-iodo-N-methylisatoic anhydride수율 78%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a mechanically stirred solution of 5-iodo-N-methylanthranilic acid (40 grams 0.144 mol), potassium carbonate (19.95 grams, 0.144 mol), and 500 ml water at 0° C. was added phosgene (1.93M solution in toluene, 0.2 mol, 104 mL) over a period of 1 hr, the resulting slurry was stirred for an additional 3 hrs and the solids isolated by filtration, washing with water, and a small amount (70 mL) of ether. The solids were dried overnight in vacuo to yield 34 grams (78%) of 5-iodo-N-methylisatoic anhydride. 1H NMR (DMSO-d6) 8.18 (1H, bs, C6-H), 8.08 (1H, bd, 3JHH=8 Hz, C4-H), 7.12 (1H, d, 3JHH=8 Hz, C3-H), 3.42 (3H, s, NCH3).

후처리

  1. customthe solids isolated by filtration
  2. washwashing with water
  3. customThe solids were dried overnight in vacuo

출처 및 근거

ORD 기록
ord-5a8578cc75214cf9b7c99710e04519c1
출처 데이터셋
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05674865

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