HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzoic Acid → HCID 86631279, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzoic Acid | HCID 6318 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 86631280 | HCID 86631280 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86631279 | HCID 86631279 | 91% |
Reaction Steps
To a solution of the compound (0.50 g) obtained in step 4, 4-chlorobenzoic acid (0.35 g) and triethylamine (0.16 mL) in acetonitrile (15 mL) were added WSC.HCl (0.43 g) and HOBt (0.34 g), and the mixture was stirred at room temperature for 14 hr. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent; 33% ethyl acetate/hexane) to give the title compound (0.42 g, 91%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470816B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-4b06fbf16d7a4a3a8c795da101d4dc33 |
| Source note | uspto-grants-2013_06 |