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Phosphorus oxychloride → Butyl 6-chloropyridazine-3-carboxylate

HRID 1870766
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HRID 1870766 반응식
P(Cl)(Cl)([Cl:3])=O.O=[C:7]1[NH:12][N:11]=[C:10]([C:13]([O:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:14])[CH:9]=[CH:8]1>C(#N)C.O>[Cl:3][C:7]1[N:12]=[N:11][C:10]([C:13]([O:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:14])=[CH:9][CH:8]=1
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참가 물질

5

반응물 2

HCID 24813Phosphorus oxychlorideHCID 12346430Butyl 1,6-dihydro-6-oxo-3-pyridazinecarboxylate

생성물 1

HCID 22622489Butyl 6-chloropyridazine-3-carboxylate수율 80%

시약·촉매·용매 2

HCID 962Water용매HCID 6342Acetonitrile용매2회

실험 절차

To a mixture of phosphorus oxychloride (20 ml) and acetonitrile (40 ml) heated at reflux was added a solution of n-butyl 6-oxo-1,6-dihydropyridazine-3-carboxylate (20 g) in acetonitrile (80 ml). The reaction was heated at reflux for 30 minutes, cooled and added to an ice cooled solution of K2C03 (87.8 g) in water (600 ml) with vigorous stirring. The product was filtered off, washed with water and dried at 60° C. to give n-butyl 6-chloropyridazine-3-carboxylate (17.5 g, 80% yield), mpt 110-111° C.

후처리

  1. temperatureheated
  2. temperatureat reflux
  3. temperatureThe reaction was heated
  4. temperatureat reflux for 30 minutes
  5. temperaturecooled
  6. filtrationThe product was filtered off
  7. washwashed with water
  8. customdried at 60° C.

출처 및 근거

ORD 기록
ord-87eff584b3e146b9828cd7e6cb639779
출처 데이터셋
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06100258

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