Triphenylphosphine → HCID 21831301, compound

HRID 1601401Notes

Reaction equation

HRID 1601401 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

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-7d3794c32b5d4cc08a020a6fc39334ce
Source dataset
uspto-grants-1999_11
Patent number
US05977167

Reaction notes

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