Water → HCID 59186922, compound

HRID 2170945Notes

Reaction equation

HRID 2170945 reaction equation
Br[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[C:4]([O:10][C:11]([F:14])([F:13])[F:12])[CH:3]=1.O.[CH3:16][N:17](C=O)C>[C-]#N.[Zn+2].[C-]#N.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH:6]([C:5]1[CH:8]=[CH:9][C:2]([C:16]#[N:17])=[CH:3][C:4]=1[O:10][C:11]([F:14])([F:13])[F:12])=[O:7]

Participants

6

Procedure

10.63 g (39.51 mmol) of 4-bromo-2-(trifluoromethoxy)benzaldehyde, 3.43 g (29.24 mmol) of zinc cyanide and 1.37 g (1.19 mmol) of tetrakis(triphenylphosphine)palladium(0) are dissolved in 80 ml of DMF. The reaction mixture is then reacted in several portions in a single mode microwave (Emrys Optimizer, 5 min at 220° C.). The combined mixtures are mixed with water and extracted twice with toluene. The combined organic phases are washed with saturated sodium chloride solution and dried with sodium sulfate, and then the solvent is removed in a rotary evaporator. The residue is purified by column chromatography (silica gel, mobile phase: cyclohexane/ethyl acetate 10:1). 3.32 g (78% of theory) of the title compound are obtained with a purity of 80% (according to LC-MS).

Workup

  1. customThe reaction mixture is then reacted in several portions in a single mode microwave (Emrys Optimizer, 5 min at 220° C.)
  2. extractionextracted twice with toluene
  3. washThe combined organic phases are washed with saturated sodium chloride solution
  4. dry with materialdried with sodium sulfate
  5. customthe solvent is removed in a rotary evaporator
  6. customThe residue is purified by column chromatography (silica gel, mobile phase: cyclohexane/ethyl acetate 10:1)

Sources & evidence

ORD record
ord-5c17c07765db4695a7970301b4e194fb
Source dataset
uspto-grants-2015_06
Patent number
US09051316B2

Reaction notes

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