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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069460Generated: October 29, 2026

Sodium hydride → 4-{[4-(4-Fluorobenzyloxy)-phenyl]-(3-methyl-butyl)-amino}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1069460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzenemethanol, 4-fluoro-, 1-methanesulfonateHCID 18380576—
Reactant4-[(4-Hydroxy-phenyl)-(3-methyl-butyl)-amino]-piperidine-1-carboxylic acid tert-butyl esterHCID 54298867—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-{[4-(4-Fluorobenzyloxy)-phenyl]-(3-methyl-butyl)-amino}-piperidine-1-carboxylic acid tert-butyl esterHCID 5446631991%

Reaction Steps

4-[(4-hydroxy-phenyl)-(3-methyl-butyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester (In, 1.18 g, 3.26 mmol) was dissolved in DMF (7 mL), treated with NaH (0.26 g, 6.52 mmol, 60% dispersion in mineral oil), and stirred for 8 minutes. 4-Fluorobenzyl methanesulfonate (Ie, 0.93 g, 4.56 mmol) was added and the reaction was stirred for 5 minutes, then diluted with EtOAc (100 mL), washed with saturated sodium bicarbonate solution and with brine, dried over Na2SO4, and concentrated. The residue was chromatographed on silica gel eluting with 4:1 hexane/EtOAc to give 1.39 g (91%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251918B1
Source datasetuspto-grants-2001_06
ORD IDord-a5ee76c4ed3444c8b1fae5621180f13f
Source noteuspto-grants-2001_06