Tributylvinyltin → HCID 54049649, compound

HRID 343944Notes

Reaction equation

HRID 343944 reaction equation
[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5](S(C(F)(F)F)(=O)=O)[CH:4]=1)#[N:2].O1C=C[CH:20]=[C:19]1P(C1OC=CC=1)C1OC=CC=1.[Cl-].[Li+].C([Sn](CCCC)(CCCC)CCCC)=C.[F-].[K+]>CN1CCCC1=O.C(OCC)C>[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5]([CH:19]=[CH2:20])[CH:4]=1)#[N:2]

Participants

8

Procedure

A mixture of 4-cyano-2-trifluoromethylsulphonyl-benzaldehyde (0.91 g, 3.26 mmol), tris(dibenzylidenacetone)dipalladium(0) (67 mg, 0.074 mmol), tris(2-furyl)phosphine (34 mg, 0.15 mmol) and anhydrous lithium chloride (0.47 g, 11.04 mmol) in dry N-methylpyrrolidinone (10 ml) was stirred under an atmosphere of nitrogen at room temperature for 5 minutes. Vinyltri-n-butyltin (1.31 g, 4.08 mmol) was added and the solution stirred at room temperature fo 22 hours. A saturated solution of potassium fluoride (15 ml) was then added, followed by diethyl ether (15 ml). After stirring for 5 minutes, the resulting yellow suspension was filtered through celite and the solids washed with diethyl ether. The filtrate layers were separated and the organic phase washed once with a saturated solution of potassium fluoride, dried, filtered and evaporated to give 4-cyano-2-vinylbenzaldehyde as a pale yellow solid.

Workup

  1. stirringthe solution stirred at room temperature
  2. waitfo 22 hours
  3. stirringAfter stirring for 5 minutes
  4. filtrationthe resulting yellow suspension was filtered through celite
  5. washthe solids washed with diethyl ether
  6. customThe filtrate layers were separated
  7. washthe organic phase washed once with a saturated solution of potassium fluoride
  8. customdried
  9. filtrationfiltered
  10. customevaporated

Sources & evidence

ORD record
ord-1ef0f6cb7d324f488954e25e7d5c0af5
Source dataset
uspto-grants-1999_01
Patent number
US05863947

Reaction notes

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