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Calcium Carbonate → 4-Amino-5-fluoro-7-iodo-1,3-benzodioxole

HRID 1785098
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HRID 1785098 반응식
[F:1][C:2]1[CH:10]=[CH:9][C:5]2[O:6][CH2:7][O:8][C:4]=2[C:3]=1[NH2:11].[I:12](Cl)(=O)=O.I(Cl)(=O)=O.C([N+](C)(C)C)C1C=CC=CC=1.C(=O)([O-])[O-].[Ca+2]>ClCCl.CO>[NH2:11][C:3]1[C:4]2[O:8][CH2:7][O:6][C:5]=2[C:9]([I:12])=[CH:10][C:2]=1[F:1]
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참가 물질

6

반응물 3

HCID 10112Calcium CarbonateHCID 179805645-fluoro-2H-1,3-benzodioxol-4-amineHCID 56924451Trimethylbenzylammonium Dichloroiodate

생성물 1

HCID 688813424-Amino-5-fluoro-7-iodo-1,3-benzodioxole수율 57.1%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344
Dichloromethane
용매

실험 절차

5-Fluoro-1,3-benzodioxol-4-amine (1.1 g, 7.10 mmol), benzyltrimethylammonium dichloroiodate (2.7 g, 7.76 mmol) and calcium carbonate (0.92 g, 9.2 mmol) in a mixture of dichloromethane (10 ml) and methanol (5 ml) were stirred at room temperature for 3 hr. The mixture was filtered through Celite and then evaporated to a dark brown solid. The residue was purified by column chromatography on silica using a 1:1 mixture of methyl tert-butyl ether and iso-hexane as eluent to give 4-amino-5-fluoro-7-iodo-1,3-benzodioxole (1.14 g, 57%) as a pale brown solid; NMR Spectrum: (CDCl3) 3.61 (s, 2H), 6.00 (s, 2H), 6.81 (d, 1H).

후처리

  1. filtrationThe mixture was filtered through Celite
  2. customevaporated to a dark brown solid
  3. customThe residue was purified by column chromatography on silica using
  4. additiona 1:1 mixture of methyl tert-butyl ether and iso-hexane as eluent

출처 및 근거

ORD 기록
ord-a0bb6e202603404c829e87cd57f5bc37
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07504408B2

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