HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 9913145, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1H-Indole, 1-ethyl-2-methyl- | HCID 170432 | — |
| Reactant | Benzoic acid, 2-[(1-ethyl-2-methyl-1H-indol-3-yl)carbonyl]- | HCID 3084978 | — |
| Reactant | HCID 70399978 | HCID 70399978 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9913145 | HCID 9913145 | — |
Reaction Steps
In a flask were charged 0.05 mol of m-diethyl-aminophenetidine and 0.05 mol of 3-(o-carboxybenzoyl)-1-ethyl-2-methylindole obtained by reacting 1-ethyl-2-methylindole and phthalic anhydride, and 0.3 mol of acetic anhydride was added thereto, followed by heating at 60° to 80° C. The reaction proceeded rapidly, and the reaction system assumed a bluish purple color. The reaction mixture was poured into water, and the precipitated crystals were collected by filtration and recrystallized from toluene to obtain the above-named compound having a melting point of 193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04803192 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-0c901fef2f224c28af42f41cd2955d8f |
| Source note | uspto-grants-1989_02 |