Propyl mercaptan → 1-(2-Bromo-1,1,2,2-tetrafluoroethoxy)-2-chloro-4-nitrobenzene

HRID 568945Notes

Reaction equation

HRID 568945 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11].C(=O)([O-])[O-].[K+].[K+].C(S)CC.Br[C:23]([F:29])([F:28])[C:24]([F:27])([F:26])[Br:25].[OH-].[Na+]>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[O:11][C:23]([F:29])([F:28])[C:24]([Br:25])([F:27])[F:26]

Participants

7

Conditions

Temperature
50 °C

Procedure

Into a pressure bottle was placed 15.0 g (0.086 mole) 2-chloro-4-nitrophenol, 11.9 g (0.086 mole) potassium carbonate, 1.5 g (0.02 mole) propanethiol, 33.7 g (0.13 mole) 1,2-dibromotetrafluoroethane and 115 ml of N,N-dimethylformamide. The pressure bottle was sealed and the mixture stirred at 50° C. for 48 hours. The pressure bottle was cooled to room temperature, opened, and the contents poured into a separatory funnel. Approximately 200 ml of a 2N sodium hydroxide solution was added to the separatory funnel. The resultant mixture was extracted with four 300 ml portions of diethyl ether. The extracts were combined and washed with two 100 ml portions of a 2N sodium hydroxide solution. The washed extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving an oil. The reaction described above was repeated three additional times. The residual oils from the four runs were combined and purified by column chromatography on silica gel, eluting with n-heptane: toluene (95:5), to yield 57.6 g of 3-chloro-4-(2-bromo-1,1,2,2-tetrafluoroethoxy)nitrobenzene as an oil.

Workup

  1. customThe pressure bottle was sealed
  2. temperatureThe pressure bottle was cooled to room temperature
  3. additionthe contents poured into a separatory funnel
  4. extractionThe resultant mixture was extracted with four 300 ml portions of diethyl ether
  5. washwashed with two 100 ml portions of a 2N sodium hydroxide solution
  6. extractionThe washed extract
  7. dry with materialwas dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customThe filtrate was evaporated under reduced pressure
  10. customleaving an oil
  11. custompurified by column chromatography on silica gel
  12. washeluting with n-heptane: toluene (95:5)

Sources & evidence

ORD record
ord-23490d3c3b124bae87ff604bb9f9fe4d
Source dataset
uspto-grants-1988_03
Patent number
US04730062

Reaction notes

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