Tributylvinyltin → HCID 15017665, compound

HRID 1682259Notes

Reaction equation

HRID 1682259 reaction equation
[F:1][C:2]1[C:11](S(C(F)(F)F)(=O)=O)=[C:10]([F:19])[C:9]([F:20])=[CH:8][C:3]=1[C:4]([O:6]C)=[O:5].[CH2:21]([Sn](CCCC)(CCCC)C=C)[CH2:22]CC.[Cl-].[Li+]>O1CCOCC1.CCOCC>[CH:21]([C:11]1[C:2]([F:1])=[C:3]([CH:8]=[C:9]([F:20])[C:10]=1[F:19])[C:4]([OH:6])=[O:5])=[CH2:22]

Participants

6

Conditions

Temperature
98 °C

Procedure

To a solution of 2,4,5-trifluoro-3-trifluoro methanesulfonyl benzoic acid, methyl ester (22.0 g, 0.065 mol) in dioxane (100 mL) was added tri-n-butyl vinyl tin (21.6 g, 0.068 mol), lithium chloride (16.7 g, 0.37 mL) 2,6-di-t-butyl-4-methylphenol (0.08 g) and palladium-tetra-triphenyl phosphine (1.1 g). The mixture was heated at 98° C. for 12 hours, cooled, diluted with ether and filtered through celite. The ether layer was concentrated and the resulting residue suspended in hexane and filtered. The filtrate was concentrated to a yellow oil which was immediately dissolved in methanol (250 mL) and 1 N sodium hydroxide (150 mL). The mixture was stirred at room temperature for 4 hours, diluted with water and ether. The aqueous layer was acidified (pH ~2) with 6 N HCl and extracted with methylene chloride. The organic layer was dried and concentrated to provide the desired product (9.6 g, 77%); mp 108°-110° C.

Workup

  1. temperaturecooled
  2. filtrationfiltered through celite
  3. concentrationThe ether layer was concentrated
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated to a yellow oil which
  6. dissolutionwas immediately dissolved in methanol (250 mL)
  7. additiondiluted with water and ether
  8. extractionextracted with methylene chloride
  9. customThe organic layer was dried
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-f80554759d1443cc994285e9fc04e16b
Source dataset
uspto-grants-1992_12
Patent number
US05175356

Reaction notes

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