HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250878Generated: November 3, 2026
Dimethylformamide → HCID 86223658, compound
https://huagongshe.com/reaction/250878
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Reactant | HCID 67273066 | HCID 67273066 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86223658 | HCID 86223658 | 86.3% |
Reaction Steps
135 mg (5 mol %) of tetrakis(triphenylphosphine)palladium are added to a solution of 800 mg (2.34 mmol, 1 eq) of 1-(3-bromophenyl)-1-ethyl-3-heptylurea and 460 mg (3.0 mmol, 1.3 eq) of 4-formylphenylboronic acid in 10 mL of a mixture of dimethylformamide and of 2M potassium phosphate solution (8/2). The reaction mixture is stirred for 3 hours at 90° C. The reaction is stopped by addition of 50 mL of water and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 740 mg of 1-ethyl-1-(4′-formylbiphenyl-3-yl)-3-heptylurea are obtained in oil form. Yield=86%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07863332B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-f78c2de464da4ceead14c1f1576f3b24 |
|---|
| Source note | uspto-grants-2011_01 |
|---|