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HCID 81430592, 화합물 → Methyl 3-bromo-5-cyanobenzoate

HRID 1771713
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HRID 1771713 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([C:12](=O)[NH2:13])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]>O=P(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([C:12]#[N:13])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]
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참가 물질

3

반응물 1

HCID 81430592HCID 81430592, 화합물

생성물 1

HCID 21942615Methyl 3-bromo-5-cyanobenzoate수율 96.4%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

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온도
100 °C

실험 절차

To methyl 3-bromo-5-carbamoyl-benzoate (2.8 g, 10.8 mmol, 1.0 eq) was added POCl3 (30 mL) and the reaction heated at 100° C. overnight. The POCl3 was removed under reduced pressure, water was added and the aqueous layer extracted with EtOAc. The combined organic extracts were dried (Na2SO4), filtered and evaporated in vacuo to afford a crude residue which was purified by column chromatography (petroleum ether:EtOAc, 20:1) to give methyl 3-bromo-5-cyano-benzoate (2.5 g, 96%). This material was dissolved in THF (30 mL) and LiOH.H2O (1.7 g, 41.6 mmol, 1.54 eq) and H2O (10 mL) were added. The mixture was stirred at room temperature overnight. The THF was removed under reduced pressure and the aqueous phase acidified with diluted HCl and extracted with EtOAc. The combined organic extracts were dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (CH2Cl2: MeOH, 50:1) to give the title compound as a white solid (2 g, 85%).

후처리

  1. customThe POCl3 was removed under reduced pressure, water
  2. additionwas added
  3. extractionthe aqueous layer extracted with EtOAc
  4. dry with materialThe combined organic extracts were dried (Na2SO4)
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customto afford a crude residue which
  8. customwas purified by column chromatography (petroleum ether:EtOAc, 20:1)

출처 및 근거

ORD 기록
ord-3546e09a696f409ba2535a6c729bdbe7
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249085B2

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