Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228577Generated: October 29, 2026

4-Methoxyphenol → HCID 23450319, compound

https://huagongshe.com/reaction/2228577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
Reactantalpha-Bromo-2-nitrotolueneHCID 77569—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23450319HCID 2345031971%

Reaction Steps

To a suspension of potassium t-butoxide (5.7 g, 51 mmol) in THF (200 mL) was added 4-methoxyphenol (6.3 g, 51 mmol). After 10 min, 2-nitrobenzyl bromide (10 g, 46 mmol) was added. After 48 h, the reaction was concentrated and the residue was dissolved in ethyl acetate, washed with 1 N citric acid (2×), brine, satd aq NaHCO3 (2×), water, and brine. The organic layer was MgSO4 dried, concentrated, triturated with ether, filtered and vacuum dried to give the title compound as an off-white solid (8.4 g, 71%); MS(FD): 259.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417200B1
Source datasetuspto-grants-2002_07
ORD IDord-bf6dc0aa272b4f92af0a6ab0da785eec
Source noteuspto-grants-2002_07