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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592815Generated: October 26, 2026

Pyridine → 1-(3-(p-Tolyloxy)phenyl)urea

https://huagongshe.com/reaction/1592815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantm-HydroxyphenylureaHCID 12796—
ReactantTolylboronic acidHCID 79799—
CatalystCupric acetateHCID 8895—
SolventTetrahydrofuranHCID 8028—
Product1-(3-(p-Tolyloxy)phenyl)ureaHCID 68909034—

Reaction Steps

1-(3-Hydroxyphenyl)urea (2.00 g), p-tolylboronic acid (3.57 g), and Cu(OAc)2 (2.63 g) were dissolved in 150 mL of THF, and 5.32 mL of pyridine was added. The reaction was stirred at room temperature overnight, then filtered through Celite with the aid of 200 mL EtOAc. The filtrate was washed with water, 0.2N CuSO4, 0.5N NaOH, and brine, and dried over Na2SO4 The solution was concentrated to a solid that was taken up in 200 mL of dichloromethane and stirred at room temperature for about 1 hour, after which time it was filtered to give 1-(3-(p-tolyloxy)phenyl)urea as white solid. The material was used in Step B without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294616B2
Source datasetuspto-grants-2007_11
ORD IDord-20fb2d00de434fcf9b988962e00ffa75
Source noteuspto-grants-2007_11