3-(Trifluoromethyl)aniline → HCID 178501727, 화합물

HRID 1805436노트

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HRID 1805436 반응식
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6].[N:12]([O-])=O.[Na+].[C:16]([O:22][CH3:23])(=[O:21])[CH2:17][C:18]([CH3:20])=[O:19].C([O-])(=O)C.[Na+]>Cl.O.C(O)C>[O:19]=[C:18]([CH3:20])[C:17](=[N:12][NH:6][C:5]1[CH:7]=[CH:8][CH:9]=[C:3]([C:2]([F:10])([F:11])[F:1])[CH:4]=1)[C:16]([O:22][CH3:23])=[O:21]

참가 물질

8

반응물 4

HCID 73753-(Trifluoromethyl)anilineHCID 7757Methyl acetoacetateHCID 517045Sodium AcetateHCID 23668193Sodium Nitrite

생성물 1

HCID 178501727HCID 178501727, 화합물수율 69.4%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매HCID 962Water용매

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온도
0 °C

실험 절차

A slurry of 3-(trifluoromethyl)aniline (16.12 g, 100 mmol) in 6 N HCl (100 mL) was cooled to 0° C. and treated dropwise with a solution of sodium nitrite (8.33 g, 121 mmol) in water (20 mL). The resulting pale yellow solution was poured into a slurry of methyl acetoacetate (11.62 g, 100 mmol) and sodium acetate (150 g) in ethanol (170 mL), pre-cooled to 0° C. The resulting orange slurry was stirred for 10 min. After that time, the product was collected by filtration and washed with water (500 mL). The crude material was dissolved in ethyl acetate (250 mL) and dried (MgSO4). The product crystallized upon concentration of the ethyl acetate to give 19.997 g (69%) of methyl 3-oxo-2-{[3-(trifluoromethyl)phenyl]hydrazono}butanoate as light yellow crystals.

후처리

  1. filtrationAfter that time, the product was collected by filtration
  2. washwashed with water (500 mL)
  3. dissolutionThe crude material was dissolved in ethyl acetate (250 mL)
  4. dry with materialdried (MgSO4)
  5. customThe product crystallized upon concentration of the ethyl acetate

출처 및 근거

ORD 기록
ord-0134115095f840afb0abbb012f98c59d
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08354411B2

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