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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70778Generated: October 29, 2026

Benzyl Bromide → HCID 71268696, compound

https://huagongshe.com/reaction/70778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant1,1-Dimethylethyl 3,6-dihydro-4-(hydroxymethyl)-1(2H)-pyridinecarboxylateHCID 22594484—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71268696HCID 7126869675%

Reaction Steps

55% sodium hydride (1.30 g) was added under ice-cooling to a THF (87 ml) solution of tert-butyl 4-(hydroxymethyl)-3,6-dihydropyridine-1(2H)-carboxylate (5.77 g), and this suspension was stirred at room temperature for 30 minutes. After ice-cooling again, benzyl bromide (5.32 g) and tetrabutylammonium iodide (1.00 g) were added thereto and stirring was performed at room temperature for 3 hours. After adding a saturated ammonium chloride aqueous solution, extraction was performed with EtOAc. A residue which was obtained by washing with saturated brine, drying over anhydrous magnesium sulfate, and concentration was purified by silica gel column chromatography (EtOAc/hexane) to obtain tert-butyl 4-[(benzyloxy)methyl]-3,6-dihydropyridine-1(2H)-carboxylate (6.16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822688B2
Source datasetuspto-grants-2014_09
ORD IDord-416bc3a3d2684821b8df0a95b0610b11
Source noteuspto-grants-2014_09