Triphenylphosphine → HCID 21831301, compound

HRID 363461Notes

Reaction equation

HRID 363461 reaction equation
[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[O:11][C:10]([CH2:14][F:15])([CH2:12][F:13])[CH:9]=[C:8](OS(C(F)(F)F)(=O)=O)[C:7]=2[CH:24]=1)#[N:2].C[Sn](C)(C)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Cl-].[Li+]>CCOCC.O1CCCC1>[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[O:11][C:10]([CH2:12][F:13])([CH2:14][F:15])[CH:9]=[C:8]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=3)[C:7]=2[CH:24]=1)#[N:2]

Participants

7

Reactant 4

HCID 11776TriphenylphosphineHCID 433294Lithium ChlorideHCID 11021057Pyridine, 2-(trimethylstannyl)-HCID 21831356HCID 21831356, compound

Product 1

HCID 21831301HCID 21831301, compoundYield 82.5%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Procedure

A mixture of 120 mg of 6-cyano-4-trifluoromethanesulfonyloxy-2,2-bisfluoromethyl-2H-1-benzopyran, 87 mg of 2-trimethylstannylpyridine, 25.4 mg of tris-dibenzylidene acetone chloroform dipalladium (O), 12.8 mg of triphenylphosphine, 110 mg of lithium chloride and 6 ml of dry tetrahydrofuran was refluxed for 6.5 hours. After cooling, ether was added and the mixture was filtered using Celite. After the organic layer of the mother liquor was washed with water and dried, the solvent was distilled off. The resultant residue was purified using silica gel column chromatography (developing solution, CH2Cl2) to obtain 80 mg of oily 6-cyano-2,2-bisfluoromethyl-4-(2-pyridyl)-2H-1-benzopyran represented by the following formula.

Workup

  1. temperaturewas refluxed for 6.5 hours
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. washAfter the organic layer of the mother liquor was washed with water
  5. customdried
  6. distillationthe solvent was distilled off
  7. customThe resultant residue was purified

Sources & evidence

ORD record
ord-3ad0fef4f5864091bdbe780c61b4ea78
Source dataset
uspto-grants-1999_02
Patent number
US05874446

Reaction notes

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