Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656908Generated: October 31, 2026

Tributylvinyltin → HCID 15017665, compound

https://huagongshe.com/reaction/1656908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantLithium ChlorideHCID 433294—
ReactantMethyl 2,4,5-trifluoro-3-[(trifluoromethyl)sulfonyl]benzoateHCID 19786470—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15017665HCID 1501766577%

Reaction Conditions

Temperature98 °C

Reaction Steps

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 1N 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 6N 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256662
Source datasetuspto-grants-1993_10
ORD IDord-a88f1b07cfc147bfb8487e0a5ed17a61
Source noteuspto-grants-1993_10