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Pyridinium chloride → 3-Hydroxy-5-methoxy4-nitrophenylacetic acid

HRID 1357864
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HRID 1357864 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:14][C:15]([OH:17])=[O:16])[CH:6]=[C:7]([O:12]C)[C:8]=1[N+:9]([O-:11])=[O:10].Cl.N1C=CC=CC=1>>[OH:12][C:7]1[CH:6]=[C:5]([CH2:14][C:15]([OH:17])=[O:16])[CH:4]=[C:3]([O:2][CH3:1])[C:8]=1[N+:9]([O-:11])=[O:10]
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참가 물질

3

반응물 2

HCID 10176127Pyridinium chlorideHCID 181881093,5-Dimethoxy-4-nitrophenylacetic acid

생성물 1

HCID 181880853-Hydroxy-5-methoxy4-nitrophenylacetic acid

반응 조건

온도
145 °C

실험 절차

A stirred mixture of 3,5-dimethoxy-4-nitrophenylacetic acid (0.4 g, Reference Example 13) and pyridine hydrochloride (6 g) was heated at 145° C., under argon, for 4 hours. The cooled reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water, then with brine, then dried and then evaporated to give a 1:1 mixture of the title compound and starting material (0.37 g) which was used without further purification.

후처리

  1. customThe cooled reaction mixture
  2. customwas partitioned between ethyl acetate and water
  3. washThe organic phase was washed with water
  4. dry with materialwith brine, then dried
  5. customevaporated
  6. customto give

출처 및 근거

ORD 기록
ord-706dd62df9ea4df4967deb8537e689d2
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06593354B2

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