Water → HCID 53999034, compound

HRID 1710009Notes

Reaction equation

HRID 1710009 reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.N12CCCN=C1CCCCC2.Br[CH2:23][CH2:24][C:25]([F:29])=[C:26]([F:28])[F:27].O>C(#N)C>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH2:23][CH2:24][C:25]([F:29])=[C:26]([F:28])[F:27])=[O:7])=[CH:4][CH:3]=1

Participants

6

Procedure

To a stirred solution of 1.6 grams (0.01 mole) of 4-chlorobenzoic acid in 35 ml of acetonitrile was added 1.5 ml (0.01 mole) of 1,8-diazabicyclo[5.4.0]-undec-7-ene, followed by 1.9 grams (0.01 mole) of 4-bromo-1,1,2-trifluoro-1-butene. The reaction mixture was heated under reflux for four hours then allowed to cool to ambient temperature. Water, 25 ml, was added to the reaction mixture, and the reaction mixture was extracted with three 20 ml portions of diethyl ether. The combined extracts were washed in succession with one 25 ml portion of water, two 25 ml portions of aqueous 5% sodium hydroxide and, finally, one 25 ml portion of water. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give 1.2 grams of (3,4,4-trifluoro-3-butenyl) 4-chlorobenzoate as an oil. The nmr and the ir spectra were consistent with the proposed structure.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureunder reflux for four hours
  3. extractionthe reaction mixture was extracted with three 20 ml portions of diethyl ether
  4. washThe combined extracts were washed in succession with one 25 ml portion of water, two 25 ml portions of aqueous 5% sodium hydroxide
  5. dry with materialThe organic layer was dried with sodium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-0034473abde7455db0e3ea0ece2b718d
Source dataset
uspto-grants-1990_08
Patent number
US04952580

Reaction notes

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