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Nitric Acid → 5-Bromo-2-methoxy-3-nitrobenzaldehyde

HRID 1349939
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HRID 1349939 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)[CH:7]=[O:8].[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:3]=[C:4]([N+:12]([O-:14])=[O:13])[C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)[CH:7]=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 906845-Bromo-2-methoxybenzaldehyde

생성물 1

HCID 210937475-Bromo-2-methoxy-3-nitrobenzaldehyde수율 57.1%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

5-Bromo-2-methoxybenzaldehyde (29.65 g, 138 mmol) was added to stirred concentrated sulfuric acid (160 mL) at −15° C. Nitric acid (70% w/w) (16 g) was added dropwise. Further stirring was allowed for 15 mins at this temperature before the mixture was poured onto crushed ice (2 L). The resulting precipitate was collected by filtration and partitioned between dichloromethane (800 mL) and saturated sodium hydrogen carbonate (1 L). The organic layer was dried (Na2SO4) and evaporated in vacuo to give the title compound (20.5 g) as a crude solid.

후처리

  1. additionwas poured
  2. filtrationThe resulting precipitate was collected by filtration
  3. custompartitioned between dichloromethane (800 mL) and saturated sodium hydrogen carbonate (1 L)
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-bf32651281b14c6ebabefb440b72bb2d
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214674B2

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