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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532715Generated: November 1, 2026

Potassium Carbonate → HCID 22666129, compound

https://huagongshe.com/reaction/1532715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylanilineHCID 32484—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant8-Bromooctanoic acidHCID 548275—
ReactantHCID 54317182HCID 54317182—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 22666129HCID 2266612974.2%

Reaction Steps

DPPA (123 mg, 0.45 mmols) was added to a DMF (1 ml) solution of 8-bromooctanoic acid (100 mg, 0.45 mmols) and potassium carbonate (68 mg, 0.49 mmols), and stirred at room temperatures for 3 hours. The reaction mixture was diluted with water, and extracted with ether. The organic layer was washed with water, and dried with anhydrous magnesium sulfate, and the solvent was evaporated. A chloroform (2 ml) solution of the resulting 8-bromooctanoic acid azide (95 mg, 0.38 mmols) was heated under reflux for 30 minutes, to which was added a chloroform (1 ml) solution of 2,6-diisopropylaniline (68 mg, 0.38 mmols), and heated under reflux for further 15 hours. After the reaction, the solvent was evaporated, and the residue was purified through preparative thin-layer chromatography (developer: chloroform/methanol=20/1) to obtain 112 mg (yield: 63%) of N-(7-bromoheptyl)-N′-(2,6-diisopropylphenyl)urea as colorless powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204278B1
Source datasetuspto-grants-2001_03
ORD IDord-0e0a2df361f147f2afbebc26cd460b58
Source noteuspto-grants-2001_03