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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260539Generated: October 30, 2026

Benzyl Bromide → HCID 67071797, compound

https://huagongshe.com/reaction/1260539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178474734HCID 178474734—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67071797HCID 67071797—

Reaction Steps

N-{3-[4-(6-Hydroxypyridin-3-yloxy)phenyl]-1-methylpropyl}acetamide (150 mg, 0.5 mmol) was stirred with potassium tert-butoxide (168 mg, 1.5 mmol) and benzylbromide (342 mg, 2 mmol) in 3 ml of NMP at room temperature for 10 h. The batch was admixed with ethyl acetate and water, and the organic phase was separated off, concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 22 mg (11%), M+H+: 391.15. N-{3-[4-(1-Benzyl-6-oxo-1,6-dihydropyridin-3-yloxy)phenyl]-1-methylpropyl}acetamide was obtained as by-product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470841B2
Source datasetuspto-grants-2013_06
ORD IDord-4a2aca712674430fa831878a4e164174
Source noteuspto-grants-2013_06