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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355387Generated: October 31, 2026

HCID 59382960, compound → HCID 67191356, compound

https://huagongshe.com/reaction/2355387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59382960HCID 59382960—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67191356HCID 67191356165.4%

Reaction Steps

A 1000-mL, three-necked flask was charged with the (2-(o-tolyloxy)phenyl)((R)-1-(tert-butoxycarbonyl)piperidin-3-yl)methanone (20 g, 0.05 mol) and THF (250 mL). The flask was evacuated and refilled with N2, the mixture was cooled with a dry ice-acetone bath and the Grignard reagent was added dropwise. The mixture was allowed to warm slowly to rt and stirred overnight. After quenching with sat'd aq NH4Cl (500 mL), the mixture was extracted with EtOAc (3×150 mL) and the combined organic layers were dried over Na2SO4. The solvent was removed and the crude product was purified by flash column chromatography to afford the (R)-tert-butyl 3-((S)-1-(2-(o-tolyloxy)phenyl)-1-hydroxy-5-methoxypentyl)piperidine-1-carboxylate (20 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-3d1dbc40c9c942118d68ed5e16b80ad3
Source noteuspto-grants-2010_07