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

HRID 41240
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인쇄 미리보기

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HRID 41240 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 this order, and the mixture was stirred at 70° C., and then isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise thereto over 10 minutes. The mixture was stirred at 70° C. for 40 minutes. The mixture was returned to room temperature, the solvent was then distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (a mixed solvent 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 stirred at 70° C. for 40 minutes
  2. customwas returned to room temperature
  3. distillationthe solvent was then distilled off under reduced pressure
  4. customthe residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate

출처 및 근거

ORD 기록
ord-02496be81bb3406ea0711670738f8315
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08530504B2

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