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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375461Generated: October 30, 2026

Sodium Carbonate → HCID 58641236, compound

https://huagongshe.com/reaction/2375461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium ChlorideHCID 433294—
Reactant(2,5-Difluorophenyl)boronic acidHCID 2734335—
ReactantHCID 59682332HCID 59682332—
CatalystHCID 178418397HCID 178418397—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
ProductHCID 58641236HCID 58641236—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a flame dried flask equipped with stir bar was added (2S)-tert-butyl 2-phenyl-4-{[(trifluoromethyl)sulfonyl]oxy}-2,5-dihydro-1H-pyrrole-1-carboxylate (6-4, 0.250 g, 0.636 mmol), 2,5-difluorophenyl boronic acid (0.251 g, 1.59 mmol), Na2CO3 (0.202 g, 1.91 mmol), and LiCl (0.081 g, 1.91 mmol). The solids were dissolved in 20 mL 4:1 DME/H2O and degassed with nitrogen. Pd(PPh3)4 (0.037 g, 0.032 mmol) was added and the reaction was sealed under nitrogen and heated to 90° C. for 2 hours. Upon completion, the reaction was partitioned between 5% aq. NaHCO3 and EtOAc (3×50 mL), and the combined organic layers were dried over MgSO4. Following filtration, the organic layer was concentrated and purified via flash column chromatography (SiO2, 0-20% EtOAc/hexanes gradient) to provide (2S)-tert-butyl 4-(2,5-difluorophenyl)-2-phenyl-2,5-dihydro-1H-pyrrole-1-carboxylate (6-5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465746B2
Source datasetuspto-grants-2008_12
ORD IDord-e8cf62e6433744f59d2a96c8fee9c29c
Source noteuspto-grants-2008_12