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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323055Generated: October 26, 2026

Triethylamine → N-(2-hydroxy-4-nitrophenyl)-N'-(2,3-methylenedioxyphenyl)urea

https://huagongshe.com/reaction/323055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1,3-Dioxaindane-4-carboxylic acidHCID 304832—
Reactant2-Amino-5-NitrophenolHCID 4984721—
SolventTolueneHCID 1140—
ProductN-(2-hydroxy-4-nitrophenyl)-N'-(2,3-methylenedioxyphenyl)ureaHCID 988343242%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of the 2,3-methylenedioxyphenylcarboxylic acid in toluene, triethylamine (0.27 mL, 1.95 mmol) and diphenylphosphoryl azide (DPPA) (0.32, mL, 1.5 mmol) were added. The reaction mixture was stirred at 60° C. for 2 hours, then 2-amino-5-nitrophenol (250 mg, 1.5 mmol) was added. The reaction mixture was stirred at 100° C. for 18 hours. After the reaction mixture was cooled to room temperature, it was partitioned between 5% citric acid and ethyl acetate. The organic layer was separated and the aqueous layer was extracted three times with ethyl acetate. The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatography of the resulting solid on silica gel (hexane:ethyl acetate; 5:1) gave product (200 mg, 42%). EI-MS m/z 318 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211373B1
Source datasetuspto-grants-2001_04
ORD IDord-ef0995265c31454f9a3e3ffc16bdabb9
Source noteuspto-grants-2001_04