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4-Fluoro-3-(trifluoromethyl)benzonitrile → HCID 67364762, 화합물

HRID 2222565
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반응식

HRID 2222565 반응식
F[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[C:10]([F:13])([F:12])[F:11].[K].CC(C)([O-])C.Cl.[NH:21]1[CH2:25][CH2:24][C:23](=[O:26])[NH:22]1>CS(C)=O>[N:21]1([C:2]2[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=2[C:10]([F:13])([F:12])[F:11])[CH2:25][CH2:24][C:23](=[O:26])[NH:22]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1442554-Fluoro-3-(trifluoromethyl)benzonitrileHCID 2733712Pyrazolidin-3-one hydrochlorideHCID 50987170Potassium tertbutoxide

생성물 1

HCID 67364762HCID 67364762, 화합물

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

실험 절차

1.00 g (5.29 mmol) 4-fluoro-3-trifluoromethyl-benzonitrile are stirred together with 1.35 g (12.0 mmol) potassium-tert.-butoxide in 4 ml DMSO at ambient temperature under an argon atmosphere for 35 min and then 1.00 g (8.16 mmol) pyrazolidin-3-on-hydrochloride in 3 ml DMSO are added. After stirring at ambient temperature for 68 h the reaction mixture is poured into semisat. sodium chloride solution and extracted with ethyl acetate. The combined organic phases are dried over magnesium sulphate and evaporated down completely i. vac.

후처리

  1. additionis poured into semisat
  2. extractionsodium chloride solution and extracted with ethyl acetate
  3. dry with materialThe combined organic phases are dried over magnesium sulphate
  4. customevaporated down completely

출처 및 근거

ORD 기록
ord-180b3008dc2248318dde89bd6692125d
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07371743B2

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