HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 54120358, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 20373189 | HCID 20373189 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54120358 | HCID 54120358 | — |
Reaction Steps
3-(2-Carbethoxy-ethyl)-4-methyl-5-carbethoxypyrrole (0.4 g (35)), 5ml of hydriodic acid, 5 ml of acetic acid, 1 ml of hypophosphorous acid and 0.23 ml of propionaldehyde were reacted as above. The solution was poured into 60 ml of water which was then brought to pH 5 with ammonia. The precipitate (of the partially hydrolyzed product) was esterified in 5 ml of 5% ethanolic HCl. The solvent was evaporated and the residue was distilled then recrystallized from pentane (0.1 g), m.p. 61.5°-63.5° C (lit. 63° - 64° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04070366 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-e3aea75115234f06b9e4d55d352b6cb3 |
| Source note | uspto-grants-1978_01 |