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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-(Methylsulfonyl)phenylboronic acid | HCID 2773542 | — |
| Reactant | trans-3-(3-Chloro-phenyl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 67001287 | — |
| Solvent | N,N-Dimethylacetamide--water (1/1) | HCID 21534740 | — |
| Product | Acetate | HCID 175 | — |
| Product | trans-3-(3'-Methanesulfonyl-biphenyl-3-yl)-4-phenyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 67000610 | 99.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063088B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-3b3dcce682b747c09f3d6655adbb1261 |
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| Source note | uspto-grants-2011_11 |
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