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Hydrochloric Acid → ethyl (2E)-3-(3-iodophenyl)acrylate

HRID 1375650
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HRID 1375650 반응식
[H-].[Na+].[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[CH:7]=O.[NH4+].[Cl-].Cl.[C:15]([O:18][CH2:19][CH3:20])(=[O:17])[CH3:16]>C1COCC1.O>[I:3][C:4]1[CH:5]=[C:6](/[CH:7]=[CH:16]/[C:15]([O:18][CH2:19][CH3:20])=[O:17])[CH:9]=[CH:10][CH:11]=1
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참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 2526103-Iodobenzaldehyde

생성물 1

HCID 15508352ethyl (2E)-3-(3-iodophenyl)acrylate

시약·촉매·용매 2

HCID 962
Water
용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a suspension of NaH (60% dispersion in mineral oil) (120 mg, 3.0 mmol) in THF (20 mL) was added triethyl phosphonoacetate (436 μL, 2.2 mmol) dropwise. 3-iodo-benzaldehyde (465 mg, 2.0 mmol) was added after the bubbling has stopped. The reaction mixture was stirred at room temperature for 15 minutes. Solid NH4Cl was added, followed by 1N HCl to quench the reaction. The mixture was taken up in ethyl acetate and water. The organic phase was washed with aqueous NaHCO3, brine, dried (MgSO4), filtered and concentrated under reduced pressure and purified by flash chromatography on silica gel with hexane/ethyl acetate (4:1) to provide the titled compound (605 mg).

후처리

  1. customto quench
  2. customthe reaction
  3. washThe organic phase was washed with aqueous NaHCO3, brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. custompurified by flash chromatography on silica gel with hexane/ethyl acetate (4:1)

출처 및 근거

ORD 기록
ord-7830f5fd47f14eb19757711483fc4a4c
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07169797B2

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