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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493399Generated: October 30, 2026

Sodium Carbonate → HCID 59157621, compound

https://huagongshe.com/reaction/493399

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 59157621HCID 5915762159%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred slurry of 613 mg (1.17 mmol) of (S)-tert-butyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(6-bromo-pyridin-3-yl)propanoate and 422 mg (2.34 mmol, 2 eq.) of 2-ethylphenylboronic acid in 20 mL of 1:1 isopropanol/toluene was added 10.0 mL of 2 M aqueous sodium carbonate solution. The reaction mixture was purged twice with argon and evacuated and then 43.2 mg (0.059 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 9 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 (3:17) as eluant (5×15 cm column), gave the expected compound as a colorless oil, 401 mg, 59% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534763B2
Source datasetuspto-grants-2009_05
ORD IDord-f203d60e67d9406ab0196a702f21136b
Source noteuspto-grants-2009_05