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Methyl iodide → HCID 13601672, 화합물

HRID 1004232
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HRID 1004232 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:9](=[O:15])/[CH:10]=[CH:11]/[C:12]([OH:14])=[O:13])[CH:5]=[CH:6][C:7]=1[Cl:8].I[CH3:17]>CN(C=O)C.C1CCN2C(=NCCC2)CC1>[CH3:17][O:13][C:12](=[O:14])/[CH:11]=[CH:10]/[C:9]([C:4]1[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=1)=[O:15]
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참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 6172511(E)-4-(3,4-dichlorophenyl)-4-oxo-but-2-enoic acid

생성물 1

HCID 13601672HCID 13601672, 화합물수율 86%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회HCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene용매

실험 절차

To an ice cooled solution of (E)-4-(3',4'-dichlorophenyl)-4-oxo-2-butenoic acid (2.4 g, 0.01 mol) in dry DMF (80 mL), DBU (1.5 mL, 0.01) was added dropwise on stirring, under nitrogen atmosphere. To the resulting stirred solution iodomethane (3.1 mL, 0.05 mol) dissolved in dry DMF (20 mL) was added dropwise over 20 min. The resulting solution was stirred at 0° C. for 1 hour and 3 hours at room temperature. The resulting reaction mixture was poured into ice-water on stirring, and the precipitate was filtered, washed with water and then with hexane. Recrystallization from diisopropyl ether/hexane provided the pure ester (2.2 g, 86%), pale yellow needles, mp. 108-109°.

후처리

  1. additionwas added dropwise over 20 min
  2. stirringThe resulting solution was stirred at 0° C. for 1 hour and 3 hours at room temperature
  3. customThe resulting reaction mixture
  4. stirringon stirring
  5. filtrationthe precipitate was filtered
  6. washwashed with water
  7. customRecrystallization from diisopropyl ether/hexane

출처 및 근거

ORD 기록
ord-8a990e93bfea45e3a99a2b7df774c564
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06048896

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