Tributylvinyltin → HCID 15017665, compound
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
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
- temperaturecooled
- filtrationfiltered through celite
- concentrationThe ether layer was concentrated
- filtrationfiltered
- concentrationThe filtrate was concentrated to a yellow oil which
- dissolutionwas immediately dissolved in methanol (250 mL)
- additiondiluted with water and ether
- extractionextracted with methylene chloride
- customThe organic layer was dried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-f80554759d1443cc994285e9fc04e16b
- Source dataset
- uspto-grants-1992_12
- Patent number
- US05175356
Reaction notes
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