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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270734Generated: November 2, 2026

Potassium Phosphate, Tribasic → 2-Chloro-4-cyclopropyl-5-methyl-6-fluoroaniline

https://huagongshe.com/reaction/1270734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant2-Chloro-4-bromo-5-methyl-6-fluoroanilineHCID 18451500—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product2-Chloro-4-cyclopropyl-5-methyl-6-fluoroanilineHCID 18451503—

Reaction Steps

2-Chloro-4-bromo-5-methyl-6-fluoroaniline (6.5 g, 27 mmol), cyclopropylboronic acid (2.8 g, 33 mmol), tetrakis (triphenylphosphine)palladium (0) (1.4 g, 1.3 mmol), potassium phosphate (20.2 g, 95 mmol) and tricyclohexylphosphine (0.77 g, 2.7 mmol) are combined and stirred in 200 mL of a 4:1 DME/water solution. The mixture is degassed by repeated alternating application of vacuum and positive nitrogen pressure (10×). The mixture is heated to reflux temperature for 2 days and then cooled to room temperature. Most of the DME is removed by rotary evaporator and the residual mixture is partitioned between Et2O (250 mL) and water (250 mL). The organic phase is washed with brine (3×250 mL), dried (MgSO4) and concentrated by rotary evaporator. The crude product is purified using flash chromatography (8% CH2Cl2/hexanes) to give 2-chloro-4-cyclopropyl-5-methyl-6-fluoroaniline as a tan oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202364B2
Source datasetuspto-grants-2007_04
ORD IDord-2baa8c18e5704287afaadc91bd50569f
Source noteuspto-grants-2007_04