HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Benzofurandione → HCID 23043607, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Benzofurandione | HCID 138333 | — |
| Reactant | 4-(3,4-Dimethoxyphenethyl)aniline | HCID 14256024 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23043607 | HCID 23043607 | 90.6% |
Reaction Steps
A mixture of 2,3-benzofurandione (Fries and Pfaffendorf, Ber, 45, 156 (1912); Valentine, Titoff, Muller, and Reichstein, Helv. Chim. Acta, 20, 883 (1937)) (10 g, 0.0675 mol) and 4-[2-(4-aminophenyl)ethyl]-1,2-dimethoxybenzene (15.6 g, 0.0606 mol) in dry tetrahydrofuran is stirred at room temperature under nitrogen for 18 hours in the dark. The solvent is removed under reduced pressure on a rotary evaporator below 35° and the resulting solid is recrystallized from tetrahydrofuran-ethanol to give 22.2 g (90.6%) of a light-yellow solid, mp 124°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939133 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-af81dc8c2b8b4f17ae91a358456997cf |
| Source note | uspto-grants-1990_07 |