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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554283Generated: October 28, 2026

Potassium Phosphate, Tribasic → Methyl 5-cyclopropyl-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/554283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
Reactantmethyl 5-bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylateHCID 66924623—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductMethyl 5-cyclopropyl-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylateHCID 6692474022%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under an argon atmosphere, a suspension of methyl 5-bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carboxylate (2.11 g), cyclopropylboronic acid (683 mg), palladium(II) acetate (69 mg), tricyclohexylphosphine (174 mg) and tripotassium phosphate (4.55 g) in toluene (27 mL)-water (1.3 mL) was stirred at 100° C. for 4 hr. After cooling, the reaction mixture was diluted with water (50 mL), and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→8:2) to give the title compound as a yellow oil (yield 406 mg, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-e2541dedacbb4bf08b72d60480eeb920
Source noteuspto-grants-2011_11