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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578781Generated: November 2, 2026

Hydrochloric Acid → HCID 68996014, compound

https://huagongshe.com/reaction/578781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-(2-methoxyphenyl)-2-methylpropan-1-oneHCID 4594749—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 58022041HCID 58022041—
Catalystpalladium(II) acetateHCID 167845—
CatalystTri-t-butylphosphine fluoroborateHCID 44558591—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68996014HCID 6899601472.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-(2-methoxyphenyl)-2-methyl-1-propanone (0.58 g), 4-bromo-2-(tert-butoxycarbonylamino)-1-fluoro -benzene (0.94 g), palladium(II) acetate (37 mg), tri(tert -butyl)phosphine tetrafluoroborate (47 mg) and sodium tert-butoxide (0.78 g) in tetrahydrofuran (10 mL) was stirred at 60° C. under an argon atmosphere overnight. To the reaction mixture was added water, and the mixture was stirred for 10 minutes. The mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with diethyl ether. The extract was washed with water and brine successively, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=95/5−85/15) to give 2-[3-(tert-butoxycarbonylamino)-4-fluorophenyl]-1-(2-methoxyphenyl)-2-methyl-1-propanone (0.91 g). To the obtained 2-[3-(tert-butoxycarbonylamino)-4-fluorophenyl]-1-(2-methoxyphenyl)-2-methyl-1-propanone (0.34 g) was added hydrochloric acid (4 mol/L ethyl acetate solution, 3 mL), and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into a saturated aqueous sodium hydrogen carbonate solution, and the resulting mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to give the title compound (0.22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040693B2
Source datasetuspto-grants-2015_05
ORD IDord-832a86c12f214c238e189177812facae
Source noteuspto-grants-2015_05