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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25130Generated: October 25, 2026

Sodium hydride → N-Cbz-4-[4-(1,4-Dioxapent-1-yl)phenyl]butylamine

https://huagongshe.com/reaction/25130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantN-Cbz4-(4-hydroxyphenyl)butylamineHCID 11637991—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductN-Cbz-4-[4-(1,4-Dioxapent-1-yl)phenyl]butylamineHCID 2256617166.7%

Reaction Steps

To a vigorously stirred solution of 29 (4 g, 0.013 mol) in anhydrous THF (150 mL) under nitrogen at 0° C. was added sodium hydride (60% dispersion in mineral oil, 0.64 g, 0.016 mol). The mixture was stirred for 15 min then tetrabutylammonium iodide (0.5 g, 0.0013 mol) and 2-bromoethyl methyl ether (2.04 g, 0.015 mol) were added and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the material was purified by column chromatography (silica gel, 10:1 methylene chloride/ethyl acetate) to provide 64 (3.1 g, 64%). 1H NMR (300 MHz, CDCl3) δ 1.60 (m, 4H), 2.59 (m, 2H), 3.23 (m, 2H), 3.45 (s, 3H), 3.77 (m, 2H), 4.10 (m, 2H), 5.13 (s, 2H), 6.88 (d, 2H), 7.08 (d, 2H), 7.47 (s, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858615B2
Source datasetuspto-grants-2005_02
ORD IDord-4a2186cd1db345cfbc7dd8289da03907
Source noteuspto-grants-2005_02