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1,2-Dibromo-1-chloro-1,2,2-trifluoroethane → 4-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

HRID 439671
Notes
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Reaction equation

HRID 439671 reaction equation
FC(=C(F)F)[CH2:3][C:4]([OH:6])=[O:5].[Cl:10][C:11]([F:17])(Br)[C:12]([F:15])([F:14])[Br:13]>[Zn]>[Br:13][C:12]([F:15])([F:14])[C:11]([Cl:10])([F:17])[CH2:3][C:4]([OH:6])=[O:5]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 96341,2-Dibromo-1-chloro-1,2,2-trifluoroethaneHCID 152391743,4,4-Trifluoro-3-butenoic acid

Product 1

HCID 109121274-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

Reagents, catalysts & solvents 1

HCID 23994ZincCatalyst

Procedure

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.

Sources & evidence

ORD record
ord-d432447635c04182847b67566a7b2364
Source dataset
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05514717

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes