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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355565Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 12968706, compound

https://huagongshe.com/reaction/1355565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 12968705HCID 12968705—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
ProductHCID 12968706HCID 12968706—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of trifluoro-methanesulfonic acid 4-[1-benzyl-3-(3-methoxy-phenyl)-piperidin-3-yl]-phenyl ester (12.9 g, 25.4 mmol) in a Parr pressure bottle in MeOH (39 mL) were added DMSO (18 mL) and triethylamine (21 mL, 151 mmol). To the reaction mixture were added palladium acetate (3.99 g, 17.8 mmol) and 1,3-bis (diphenylphosphino) propane (5.25 g, 12.3 mmol). The mixture was shaken under 40 psi of CO at 70° C. for 4 hours. The 1n reaction mixture was cooled to room temperature and was diluted with diethyl ether (600 mL). The ether layer was washed with water (5×60 mL), dried (MgSO4) and concentrated. The crude residue was purified by flash chromatography with hexanes/EtOAc (3:1) to afford 9.82 g of 4-[1-benzyl-3-(3-methoxy-phenyl)-piperidin-3-yl]-benzoic acid methyl ester. 1HNMR (400 MHz, CDCl3) δ 7.87 (d, 2H), 7.41-7.20 (comp, 7H), 7.12 (t, 1H), 6.77 (s, 1H), 6.73 (d, 1H), 6.66 (d, 1H), 3.86 (s, 3H), 3.71 (s, 3H), 3.51 (s, 2H), 3.05 (br, 1H), 2.68 (br, 1H), 2.55 (br, 1H), 2.41-2.24 (comp, 2H), 2.22-2.18 (m, 1H) 1.61-1.42 (comp, 2H); MS (M+1) 416.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586431B1
Source datasetuspto-grants-2003_07
ORD IDord-ab1ff4e8fb154dbeb64d544d2eeaa7bf
Source noteuspto-grants-2003_07