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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515180Generated: October 30, 2026

Toluene → HCID 86699748, compound

https://huagongshe.com/reaction/515180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium BromideHCID 253877—
ReactantPotassium FluorideHCID 522689—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 86699749HCID 86699749—
ProductHCID 86699748HCID 8669974885%

Reaction Steps

A solution of 2-methyl-4-morpholin-4-yl-6-(trifluoromethylsulfonyl)oxy-benzoic acid ethyl ester (0.7 g, 1.76 mmol), potassium fluoride (0.43 g, 7.41 mmol), potassium bromide (0.25 g, 2.12 mmol) and cyclopropylboronic acid (0.30 g, 3.53 mmol) in dry toluene (16 ml) is degassed and flushed with argon for 20 min. To the reaction mixture is added tetrakis(triphenylphosphin)palladium(0) (0.20 g, 0.18 mmol) and subjected to microwave irradiation at 120° C. for 1 h. The reaction mixture is poured onto ice and extracted with ethyl acetate (3×30 ml). The combined organic layers are washed with water (20 ml), brine (20 ml) and dried over sodium sulfate. The solvent is evaporated to get the crude product, which is purified by column chromatography (silica gel, 8% acetone/hexane) to afford 2-cyclopropyl-6-methyl-4-morpholin-4-yl-benzoic acid ethyl ester (0.46 g, 1.59 mmol, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-652a751bb2b4411b8285909a2daa32f1
Source noteuspto-grants-2015_08