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Ammonia → 3,3,3-Trifluoro-2,2-dimethyl-propionamide

HRID 1807702
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HRID 1807702 반응식
[F:1][C:2]([F:10])([F:9])[C:3]([CH3:8])([CH3:7])[C:4](O)=[O:5].C(C1NC=CN=1)(C1[NH:14]C=CN=1)=O.N.C(OCC)C>C(Cl)Cl>[F:1][C:2]([F:10])([F:9])[C:3]([CH3:8])([CH3:7])[C:4]([NH2:14])=[O:5]
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참가 물질

6

반응물 4

HCID 222AmmoniaHCID 3283Diethyl EtherHCID 5250894Bis-(1H-imidazol-2-YL)-methanoneHCID 198673673,3,3-Trifluoro-2,2-dimethylpropanoic acid

생성물 1

HCID 575162793,3,3-Trifluoro-2,2-dimethyl-propionamide수율 57.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 2 g (12.81 mmol) 3,3,3-trifluoro-2,2-dimethylpropionic acid (Aldrich), 2.077 g (12.81 mmol) carbonyl-diimidazole and 5.55 ml (64.1 mmol) aqueous ammonia in 50 ml CH2Cl2 was stirred at room temperature for 20 h. After that, diethyl ether was added and the resulting mixture was washed with 0.1 N HCL, 0.1 N NaOH, water and brine. The organic layer was dried (MgSO4), filtered and concentrated in vacuo to afford 1.15 g of the title compound as white crystals, that were used in the next step without further purification. MS: M+H=156.

후처리

  1. washthe resulting mixture was washed with 0.1 N HCL, 0.1 N NaOH, water and brine
  2. dry with materialThe organic layer was dried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-60b2759cdcc14fb2accc5b31f498f7cd
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08357707B2

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