HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → HCID 5055125, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Paraldehyde | HCID 31264 | — |
| Reactant | Ethyl 2,4-dimethyl-1H-pyrrole-3-carboxylate | HCID 137481 | — |
| Reactant | Phosphonium iodide ((PH4)I) | HCID 166618 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Hydrogen iodide | HCID 24841 | — |
| Solvent | Phosphinic Acid | HCID 4124402 | — |
| Product | HCID 5055125 | HCID 5055125 | 53% |
Reaction Steps
2,4-Dimethyl-3-carbethoxy-pyrrole (0.668 g) was dissolved in a mixture of hydriodic acid (10 ml), acetic anhydride (10 ml) and hypophosphorous acid (2 ml). Paraldehyde (0.75 ml) was added. The solution was stirred 5 min., decolorized with phosphonium iodide, and poured into ice water. The cooled mixture was brought to pH 8 with ammonium hydroxide. The product was filtered off and distilled (90°-100°, 5 × 10-4 mm), giving colourless crystals (53%), m.p. 108°-109° after changing to prisms at 105°. For analysis, it was recrystallized from hexane as prismatic rods, m.p. 107°-109° (lit17) 106°-107°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04070366 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-a988550e61104924bc29383beb0b54e5 |
| Source note | uspto-grants-1978_01 |