Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507048Generated: October 26, 2026

Tributylvinyltin → 2-Amino-4-trifluoromethyl-5-vinyl-benzoic acid methyl ester

https://huagongshe.com/reaction/507048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantMethyl 2-amino-5-iodo-4-(trifluoromethyl)benzoateHCID 53436880—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-Amino-4-trifluoromethyl-5-vinyl-benzoic acid methyl esterHCID 5943248971.2%

Reaction Steps

Add tetrakis palladium(triphenylphosphine)(0) (5.00 g, 4.33 mmol) to a mixture of 2-amino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester (Example 3, Step 3) (17.25 g, 49.99 mmol) and tributyl(vinyl)tin (16.10 mL, 55.14 mmol) in toluene (500 mL) and heat at reflux for 14 h. Allow the reaction to cool to room temperature dilute the mixture with ethyl acetate (1 L). Wash the mixture with saturated aqueous potassium fluoride solution (3×300 mL), then water (300 mL), followed by brine (500 mL). Dry the organic layer over anhydrous sodium sulfate, filter, and remove the solvents under reduced pressure. Purify the residue by column chromatography on silica gel, eluting with ethyl acetate/hexanes (0 to 15%), to provide the title compound as a pale yellow solid (8.73 g, 71%): TLC Rf 0.52 (3:1 hexanes/ethyl acetate); 1H NMR (CDCl3, 300 MHz) δ 3.89 (s, 3H), 5.21-5.30 (m, 1H), 5.60-5.71 (m, 1H), 5.98 (bs, 2H), 6.83-7.02 (m, 2H), 8.19 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786108B2
Source datasetuspto-grants-2010_08
ORD IDord-8e965c236ce949aa921e75e05d2b380c
Source noteuspto-grants-2010_08