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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473778Generated: October 30, 2026

Benzyl Bromide → HCID 67007388, compound

https://huagongshe.com/reaction/473778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 59674890HCID 59674890—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67007388HCID 67007388—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of tert-butyl 5,6-dihydro-4-(3-hydroxyphenyl)pyridine-1(2H)-carboxylate (crude, 100 mg) and potassium carbonate (300 mg) in DMF was added benzyl bromide (60 μL) at room temperature. The resulting mixture was stirred at 80° C. for 16 h. The mixture was cooled down, diluted with ethyl acetate, washed with water, brine, dried and concentrated. The product (60 mg) was purified by combiflash using hexane/ethyl acetate (max. EtOAc 10%) to afford tert-butyl 4-(3-(benzyloxy)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate which was then converted to the final compound using procedures analogous to those for example 1. MS(ESI): (M+H)+=462.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637497B2
Source datasetuspto-grants-2014_01
ORD IDord-5eec213a4a5f4ce7a213115034e9b36d
Source noteuspto-grants-2014_01