HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenemethanamine, 2,5-dichloro- → 3-tert-Butylamino-4-(2,5-dichloro-benzylamino)-cyclobut-3-ene-1,2-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenemethanamine, 2,5-dichloro- | HCID 457600 | — |
| Reactant | 3-Butoxy-4-tert-butylamino-cyclobut-3-ene-1,2-dione | HCID 17819389 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-tert-Butylamino-4-(2,5-dichloro-benzylamino)-cyclobut-3-ene-1,2-dione | HCID 17819374 | 52.1% |
Reaction Steps
Employing the procedure of Example 2, Step 4, and a reaction period of 23 hours, 2,5-dichlorobenzylamine (0.88 g, 5 mmol) and 3-butoxy-4-tert-butylamino-cyclobut-3-ene-1,2-dione (1. 13 g, 5 mmol) in tetrahydrofuran (15 mL ) were converted to 1.52 g of a cream-colored solid. Recrystallization of this material from acetonitrile (twice) and from methanol provided 0.853 g of the tide compound as a white solid: mp 236° C. (softens 216° C.). MS (m/z) 326/328/330 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780505 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-049eba72c43d4e48bd0c64b358fa8146 |
| Source note | uspto-grants-1998_07 |