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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220260Generated: October 31, 2026

Sodium Carbonate → HCID 59157624, compound

https://huagongshe.com/reaction/2220260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Ethylphenylboronic Acid (contains varying amounts of Anhydride)HCID 4100862—
ReactantHCID 86609631HCID 86609631—
SolventToluene isopropyl alcoholHCID 21881414—
ProductHCID 59157624HCID 5915762477%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred slurry of 1.75 g (3.35 mmol) of (S)-tert-butyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(6-bromo-pyridin-3-yl)propanoate and 1.005 g (6.70 mmol, 2 eq.) of 2-ethylphenylboronic acid in 50 mL of 1:1 isopropanol/toluene was added 25.0 mL of 2 M aqueous sodium carbonate solution. The reaction mixture was purged twice with argon and evacuated and then 124 mg (0.167 mmol, 0.05 equivalents) of bis(tricyclohexylphosphine)palladium (II) chloride was added and the mixture was again purged with argon and evacuated. The rapidly stirred mixture was heated at 80° C. under argon. After 20 h, the reaction mixture was cooled to room temperature and partially concentrated to remove isopropanol. The residue was partitioned between ethyl acetate and water and the aqueous phase was extracted once more with ethyl acetate. The organic extracts were combined, dried over magnesium sulfate, filtered and concentrated to give a brown oil. Purification by chromatography on silica gel using ethyl acetate/dichloromethane (1:9) as eluant (5×15 cm column), gave the desired compound as a colorless oil, 1.25 g, 77% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417028B2
Source datasetuspto-grants-2008_08
ORD IDord-2afa4e05a7ec463f96a654f391baba65
Source noteuspto-grants-2008_08