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Dimethylformamide → HCID 18923653, 화합물

HRID 1899983
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HRID 1899983 반응식
P(Cl)(Cl)(Cl)=O.[CH2:6]([N:13]([CH3:22])[C:14]1[CH:19]=[C:18]([Cl:20])[CH:17]=[C:16]([Cl:21])[CH:15]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[OH-].[Na+].CN(C)[CH:27]=[O:28]>>[CH2:6]([N:13]([CH3:22])[C:14]1[CH:15]=[C:16]([Cl:21])[C:17]([CH:27]=[O:28])=[C:18]([Cl:20])[CH:19]=1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6228Dimethylformamide2회HCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 18923724HCID 18923724, 화합물

생성물 1

HCID 18923653HCID 18923653, 화합물

실험 절차

Phosphoryl chloride (12.7 ml) was dropwise added to N,N-dimethylformamide (70 ml), and the mixture was stirred for 30 minutes at ambient temperature. A solution of N-benzyl-3,5-dichloro-N-methylaniline (7.26 g) in N,N-dimethylformamide (30 ml) was dropwise added thereto, and the mixture was stirred for 30 minutes at ambient temperature and then for 30 minutes at 50° C. The reaction mixture was neutralized with 1N aqueous sodium hydroxide solution and extracted with ethyl acetate. The organic solution was washed with water and brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by a flash chromatography (ethyl acetate:n-hexane=1:6, V/V) to give N-benzyl-3,5-dichloro-4-formyl-N-methylaniline (5.70 g).

후처리

  1. stirringthe mixture was stirred for 30 minutes at ambient temperature
  2. waitfor 30 minutes at 50° C
  3. extractionextracted with ethyl acetate
  4. washThe organic solution was washed with water and brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by a flash chromatography (ethyl acetate:n-hexane=1:6, V/V)

출처 및 근거

ORD 기록
ord-6709f17ea3bb4106bcdc53d580da623b
출처 데이터셋
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05574042

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