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Ethanol → Ethyl 3-iodo-2-methylbenzoate

HRID 409194
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HRID 409194 반응식
[I:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].S(Cl)(Cl)=O.[CH2:16](O)[CH3:17]>>[CH2:16]([O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][CH:10]=[C:2]([I:1])[C:3]=1[CH3:11])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 27348883-Iodo-2-methylbenzoic acid

생성물 1

HCID 54051219Ethyl 3-iodo-2-methylbenzoate

실험 절차

To a stirred solution of 3-iodo-2-methyl-benzoic acid (30 g, 0.11 mol) in ethanol (425 mL) was added thionyl chloride (42 mL, 0.57 mol) at 0° C. The mixture was refluxed for 4.5 h before it was cooled to room temperature and concentrated in vacuo. The residue was partitioned between ethyl ether and saturated sodium bicarbonate solution. The organic layer was washed with brine, dried over anhydrous sodium sulfate and was concentrated in vacuo to give the title compound as a pale yellow oil (32.28 g): 1H NMR (CDCl3, 200 MHz): δ=7.94 (d, J=7.8 Hz, 1H), 7.70 (d, J=7.4 Hz, 1H), 6.90 (t, J=7.8 Hz, 1H), 4.35 (q, J=7.2 Hz, 2H), 2.65 (s, 3H), 1.38 (t, J=7.0 Hz, 3H).

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The mixture was refluxed for 4.5 h before it
  • concentrationconcentrated in vacuo
  • customThe residue was partitioned between ethyl ether and saturated sodium bicarbonate solution
  • washThe organic layer was washed with brine
  • dry with materialdried over anhydrous sodium sulfate
  • concentrationwas concentrated in vacuo
  • 출처 및 근거

    ORD 기록
    ord-aa1a8642cb36441381b1f7047bef1e3f
    출처 데이터셋
    uspto-grants-2014_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08759373B2

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