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Acetonitrile → Ethyl 3-chloro-4-iodo-5-methoxybenzoate

HRID 1971777
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HRID 1971777 반응식
N[C:2]1[C:12]([O:13][CH3:14])=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][C:3]=1[Cl:15].C(#N)C.[I:19]CI.N(OCCC(C)C)=O>CCCCCCC.C(OCC)(=O)C>[Cl:15][C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([O:13][CH3:14])[C:2]=1[I:19])[C:6]([O:8][CH2:9][CH3:10])=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6342AcetonitrileHCID 6346DiiodomethaneHCID 8053Isoamyl NitriteHCID 57912463Ethyl 4-amino-3-chloro-5-methoxybenzoate

생성물 1

HCID 57912451Ethyl 3-chloro-4-iodo-5-methoxybenzoate수율 66.6%

시약·촉매·용매 1

HCID 21899848Ethylacetate heptane
용매

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온도
70 °C

실험 절차

To ethyl 4-amino-3-chloro-5-methoxybenzoate (15.8 g, 68.8 mmol) were added acetonitrile (40 mL) and diiodomethane (22.2 mL, 275 mmol) in that order, and then the mixture was stirred at 70° C. and isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise over a period of 10 minutes. The mixture was then stirred at 70° C. for 40 minutes. After returning the mixture to room temperature, the solvent in the mixture was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (mixture of n-heptane and ethyl acetate: n-heptane/ethyl acetate=8/1 then 5/1) to obtain the title compound (15.6 g, 45.8 mmol).

후처리

  1. stirringThe mixture was then stirred at 70° C. for 40 minutes
  2. customto room temperature
  3. distillationthe solvent in the mixture was distilled off under reduced pressure
  4. customthe residue was purified by silica gel column chromatography (
  5. additionmixture of n-heptane and ethyl acetate

출처 및 근거

ORD 기록
ord-cfae15e6fc0f46c9a0f38139eac18d33
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431603B2

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