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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912874Generated: October 25, 2026

4-Bromo-3-(trifluoromethyl)aniline → 3-Trifluoromethyl-4-vinylaniline

https://huagongshe.com/reaction/1912874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-(trifluoromethyl)anilineHCID 67852—
ReactantPotassium trifluorovinylborateHCID 86620274—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTert-ButylamineHCID 6385—
Product3-Trifluoromethyl-4-vinylanilineHCID 2315517279.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

In 20 mL of isopropanol, 10 mL of water and 5 mL of t-butylamine, 4.0 g (16.7 mmol) of 4-bromo-3-(trifluoromethyl)aniline was dissolved, and 4.0 g (29.9 mmol) of potassium (trifluoro)vinylborate and 300 mg (0.37 mmol) of PdCl2(dppf)2•2(dichloromethane) complex were added thereto, and the mixture solution was stirred in an argon atmosphere at 80° C. for 20 hours. The reaction solution was concentrated and the residue was partitioned between water and ethyl acetate, and the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The product was purified by a silica gel column (n-hexane:ethyl acetate=6:1) to obtain 2.475 g (79%) of a target product as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-744a22c9d51640a2a06e84a07a95c9aa
Source noteuspto-grants-2013_12