HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532715Generated: November 1, 2026
Potassium Carbonate → HCID 22666129, compound
https://huagongshe.com/reaction/1532715
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diisopropylaniline | HCID 32484 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 8-Bromooctanoic acid | HCID 548275 | — |
| Reactant | HCID 54317182 | HCID 54317182 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22666129 | HCID 22666129 | 74.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204278B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-0e0a2df361f147f2afbebc26cd460b58 |
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| Source note | uspto-grants-2001_03 |
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