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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874944Generated: October 26, 2026

Potassium Phosphate, Tribasic → Methyl 1-(4-phenylthiazol-2-yl)pyrrolidine-3-carboxylate

https://huagongshe.com/reaction/874944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantMethyl Pyrrolidine-3-carboxylateHCID 4114360—
Reactant2-Bromo-4-phenyl-1,3-thiazoleHCID 9921106—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductMethyl 1-(4-phenylthiazol-2-yl)pyrrolidine-3-carboxylateHCID 6732374773%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-bromo-4-phenylthiazole (300 mg, 1.25 mmol) and pyrrolidine-3-carboxylic acid methyl ester (177 mg, 1.37 mmol) and potassium phosphate (290 mg, 1.37 mmol) in dry toluene (5 mL) were taken in a sealed tube and purged argon gas for 10 min. A catalytic amount of tri-tert-butylphosphine (12 mg, 0.06 mmol) was added, followed by palladium acetate (15 mg, 0.06 mmol), and the reaction mixture was heated to 80° C. for 10 h. The reaction mixture was then filtered through Celite and the clear filtrate was concentrated under reduced pressure to get the crude product which was purified by column chromatography (silica 60-120 mesh, eluant 15-18% EtOAc in petroleum ether) to get methyl 1-(4-phenylthiazol-2-yl)pyrrolidine-3-carboxylate (75 mg, yield 73%). 1H NMR (300 MHz, CDCl3) δ 7.87-7.83 (m, 2H), 7.44-7.31 (m, 4H), 3.88-3.78 (m, 2H), 3.75 (s, 3H), 3.70-3.67 (m, 1H), 3.61-3.55 (m, 1H), 3.32-3.23 (m, 1H), 2.41-2.32 (m, 2H). MS (ESI) m/z: Calculated for C16H16N2O2S: 288.09. found: 289.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981084B2
Source datasetuspto-grants-2015_03
ORD IDord-25a054d8ac304921a587c696fbf8589e
Source noteuspto-grants-2015_03