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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509374Generated: October 25, 2026

Potassium Phosphate, Tribasic → HCID 86687981, compound

https://huagongshe.com/reaction/509374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantVinylboronic acidHCID 4683185—
Reactant(4-(N,N-Dimethylamino)phenyl)di-tert-butyl phosphineHCID 11714598—
Reactant(S)-tert-butyl((3-bromopyridin-2-yl)(4-(trifluoromethyl)phenyl)methyl)carbamateHCID 71164782—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86687981HCID 86687981—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of (S)-tert-butyl ((3-bromopyridin-2-yl)(4-(trifluoromethyl)-phenyl)methyl)carbamate (0.4 g, 0.93 mmol) in water (2 mL) and EtOH (8 mL) were added K3PO4 (0.3 g, 1.3 mmol), vinyl boronic acid (4 mL, 9.3 mmol) and A−taPhos)2PdCl2 (Guram, A. S. et al. Org. Lett. 2006, 8, 1787; 0.13 g, 0.01 mmol). The resulting mixture was stirred at 120° C. for 1 h. Reaction progress was monitored by TLC (20% EtOAc in petroleum ether). After completion of reaction, water (50 mL) was added to the reaction mixture, and the product was extracted with DCM (3×25 mL). The combined organic layers were separated, dried over anhydrous sodium sulfate, and purified by column chromatography using silica (100-200 mesh) and using 15-30% EtOAc in petroleum ether as an eluent. In this manner, (S)-tert-butyl ((4-(trifluoromethyl)phenyl)(3-vinylpyridin-2-yl)methyl)carbamate was obtained as an off-white solid. MS (ESI pos. ion) m/z: 378.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096527B2
Source datasetuspto-grants-2015_08
ORD IDord-a0fb20d6c345436db1e95824f6aadeea
Source noteuspto-grants-2015_08