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Water → 3,4-Dichloro-3,4,4-trifluorobutanoic acid

HRID 439670
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HRID 439670 반응식
[Cl:1][C:2]([F:8])(Cl)[C:3]([F:6])([F:5])[Cl:4].[C:9](Cl)(Cl)=C.S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].[CH:25]([O-:27])=[O:26].[Na+].O.C(=O)=O.CC(C)=O>CN(C=O)C>[Cl:1][C:2]([F:8])([C:3]([Cl:4])([F:6])[F:5])[CH2:9][C:25]([OH:27])=[O:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 962WaterHCID 6366Vinylidene chlorideHCID 6428Cfc 113HCID 62648Ammonium PersulfateHCID 2723810Sodium FormateHCID 18522661Acetone cardice

생성물 1

HCID 218364853,4-Dichloro-3,4,4-trifluorobutanoic acid

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 1,1,2-trichlorotrifluoroethane (X) (9.37 g, 50 mmol), vinylidene chloride (4.85 g, 50 mmol), ammonium persulfate (11.41 g, 50 mmol), sodium formate (3.4 g, 50 mmol) and water (1.8 g, 0.1 mol) in DMF (80 mL.) was stirred (dry-ice/acetone condensor) at room temperature with air bubbling. After 30 min, an aliquot of the reaction mixture was acidified with dilute HCl, extracted with ether and analyzed by GC, which indicated the formation of two products. These products were identified by GC/MS (EI) as 4-chloro-3,4,4-trifluoro-2-butenoic acid and novel compound 3,4-dichloro-3,4,4-trifluorobutanoic acid (XI). The compound XI gives 3,4,4-trifluoro-3-butenoic add (IV) upon reaction with zinc. Under the above reaction conditions, 1-chloro-1,2-dibromotrifluoroethane (VI) gave 3-chloro-4-bromo-3,4,4-trifluorobutanoic acid (VIII) as one of the products.

후처리

  1. custombubbling
  2. extractionextracted with ether

출처 및 근거

ORD 기록
ord-25e552637f484c7c974664d26f02bba0
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05514717

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