HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(1,1-Dimethyl-propylamino)-4-(2,4,6-trimethyl-benzylamino)-cyclobut-3-ene-1,2-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2,4,6-Trimethylphenyl)methanamine hydrochloride | HCID 458432 | — |
| Reactant | 3-Butoxy-4-(1,1-dimethylpropylamino)-cyclobut-3-ene-1,2-dione | HCID 15838837 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1,1-Dimethyl-propylamino)-4-(2,4,6-trimethyl-benzylamino)-cyclobut-3-ene-1,2-dione | HCID 10495490 | 42.2% |
Reaction Steps
Tetrahydrofuran (15 mL), 3-butoxy-4-(1,1-dimethyl-propylamino)-cyclobut-3-ene-1,2-dione (1,20 g, 5 mmol), 2,4,6-trimethylbenzylamine hydrochloride (0.928 g, 5 mmol, Example 9, Step 2) and triethylamine (0.506 g, 5 mmol) were stirred together at room temperature for 3 days. The mixture was then prepared as in Example 9, Step 3. Three recrystallization of the crude product from acetonitrile provided 0.664 g of the title compound as a white solid: mp 284°-5° C. (dec) (softens 282° C.). MS (m/z) 314 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780505 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-a74bd2805e124a75b5371431db41b9e6 |
| Source note | uspto-grants-1998_07 |