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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560123Generated: October 25, 2026

Water → trans-3-(3'-Methanesulfonyl-biphenyl-3-yl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/560123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
Reactanttrans-3-(3-Chloro-phenyl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl esterHCID 67001287—
SolventN,N-Dimethylacetamide--water (1/1)HCID 21534740—
ProductAcetateHCID 175—
Producttrans-3-(3'-Methanesulfonyl-biphenyl-3-yl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl esterHCID 6700061099.9%

Reaction Steps

To a solution of trans-3-(3-chloro-phenyl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl ester (50 mg) and 3-(methylsulfonyl)phenylboronic acid (40.3 mg) in a mixture of DMA/water (1.1 mL, 10:1) was added Cs2CO3 (87.6 mg) and [(t-Bu)2P(OH)]2PdCl2 (POPd) (8.1 mg). The reaction mixture was irradiated with microwave at 90° C. for 10 min, and at 140° C. for 10 and 15 min. Water was added, the phases were separated, and the inorganic one was extracted with ethyl acetate (×2). The organic layers were combined, washed with brine, dried (Na2SO4) and concentrated in vacuo. Column chromatography (SiO2, n-heptanelethyl acetate 1:1, and on ISOLUTE Flash NH2, n-heptane/ethyl acetate 3:1) yielded trans-3-(3′-methanesulfonyl-biphenyl-3-yl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl ester (33 mg, 49%) as a colorless oil, MS: 509.3 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063088B2
Source datasetuspto-grants-2011_11
ORD IDord-3b3dcce682b747c09f3d6655adbb1261
Source noteuspto-grants-2011_11