HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 21504746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 21504756 | HCID 21504756 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hydrogen iodide | HCID 24841 | — |
| Product | HCID 21504746 | HCID 21504746 | — |
Reaction Steps
2.5 gm (0.007 mol) of 2-carboxy-4-oxo-6,6-dimethyl-8-methoxy-4H,6H-[2]-benzopyrano-[3,4-f]-[1]-benzopyran, prepared as described in Example 2, were refluxed for 4 hours in 50 ml of hydroiodic acid. Then, the reaction mixture was cooled and diluted with 200 ml of water. The precipitated yellow crystals were filtered off, washed with water, dried and recrystallized from methanol. 250 gm (10.5% of theory) of the compound named in the heading, m.p. 256°-258° C, were obtained. The ethanolamine salt, prepared in analogy with Example 1, had a melting point of 200°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987186 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-6ee051771d5647d89f7e781d39e716fe |
| Source note | uspto-grants-1976_10 |