HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-(1-Ethyl-2-methylindol-3-yl)-3-(1-methyl-2-naphthylindolizin-3-yl)phthalide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Benzoic acid, 2-[(1-ethyl-2-methyl-1H-indol-3-yl)carbonyl]- | HCID 3084978 | — |
| Reactant | 1-Methyl-2-(2-naphthyl) indolizine | HCID 20536960 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(1-Ethyl-2-methylindol-3-yl)-3-(1-methyl-2-naphthylindolizin-3-yl)phthalide | HCID 20536950 | — |
Reaction Steps
A mixture of 3.0 grams of (1-ethyl-2-methylindol-3-yl) (2-carboxyphenyl)ketone, 2.5 grams of 1-methyl-2-(2-naphthyl) indolizine and 10 ml. of acetic anhydride was heated at 39° C. for about two hours. The resulting solution was cooled and added to a mixture of ice, toluene and ammonia. The toluene layer was separated, dried, treated with charcoal and filtered. Petroleum ether was added and after fractional precipitation a crystalline product was obtained and recrystallized from a toluene-heptane mixture to a constant melting point of 191°-193° C. A chloroform solution of this final product gave a blue color when applied to a record sheet material coated with a zinc-modified phenolic resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232887 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-0e002ee84a934afaaaca5e2dd62aa110 |
| Source note | uspto-grants-1980_11 |