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Methanol → Methyl 4-(allyloxy)-5-bromo-2-chlorobenzoate

HRID 2206694
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HRID 2206694 반응식
[CH2:1]([O:4][C:5]1[C:13]([Br:14])=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[C:7]([Cl:15])[CH:6]=1)[CH:2]=[CH2:3].O=S(Cl)Cl.[CH3:20]O>>[CH2:1]([O:4][C:5]1[C:13]([Br:14])=[CH:12][C:8]([C:9]([O:11][CH3:20])=[O:10])=[C:7]([Cl:15])[CH:6]=1)[CH:2]=[CH2:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 533294054-(Allyloxy)-5-bromo-2-chlorobenzoic acid

생성물 1

HCID 86714037Methyl 4-(allyloxy)-5-bromo-2-chlorobenzoate수율 99%

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온도
0 °C

실험 절차

To a solution of compound 21 (17.0 g, 58.0 mmol) in MeOH (380 mL) was added dropwise SOCl2 (21.1 mL, 291 mmol) at 0° C. under an atmosphere of nitrogen. The mixture was stirred at 0° C. for 30 min and then, stirred at 0° C. for 14 hours. The mixture was concentrated in vacuo and poured into aq. saturated NaHCO3 solution and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide the crude product 39 (17.7 g, 99%) as a white solid.

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후처리

  1. stirringstirred at 0° C. for 14 hours
  2. concentrationThe mixture was concentrated in vacuo
  3. additionpoured into aq. saturated NaHCO3 solution
  4. extractionextracted with EtOAc
  5. washThe organic layer was washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-cd42639a16ae4904a72be7bf3b771da0
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371303B2

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