HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 12094482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Acetylbenzoic Acid | HCID 11470 | — |
| Reactant | 3,3-Dimethylbutylamine | HCID 19709 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 12094482 | HCID 12094482 | 65.8% |
Reaction Steps
4-Acetylbenzoic acid (200 mg, 1.20 mmol) and amine 2 (from Example 1, 199 mg, 1.22 mmol) were dissolved in 5 mL of dichloromethane and triethylamine (187 μL, 1.34 mmol) and 4-dimethylaminopyridine (15 mg, 0.12 mmol) were added. 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (398 mg, 1.34 mmol) was added and the mixture was stirred for 18 hours. The reaction was diluted with ethyl acetate and washed with hydrochloric acid (1.0 M, aq.), sodium bicarbonate (sat'd., aq.) and sodium chloride (sat'd., aq.). The organic layer was dried over magnesium sulfate, filtered and the solvent removed to yield 216 mg (65%) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06624309B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-808bc8a646a64a22b7cf3a932bd7b712 |
| Source note | uspto-grants-2003_09 |