Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 20515473 | HCID 20515473 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 20515428 | HCID 20515428 | — |
Reaction Steps
The solution of 61 g (0.19 mole) of potassium 1,4,5-trimethyl-3-[(2-nitrophenyl)amino]-1H-pyrrole-2-carboxylate obtained in Example 3 is adjusted to pH 2 with concentrated hydrochloric acid in a circulatory hydrogenation apparatus, and 0.5 g of palladium-on-charcoal (10%) is added. When the internal temperature reaches 40° C., hydrogenation is started. Sufficient hydrogen is metered to keep the internal temperature at about 100° C. When a sudden drop in the absorption of hydrogen is observed, the solution is allowed to cool; it is filtered under nitrogen, and the residue on the filter is washed 6 times with 5 ml of 1-methyl-2-pyrrolidone each time. The combined filtrates are concentrated to half their volume on a rotary evaporator. The resulting solution is subsequently processed in Example 5 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04363816 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-99cb363d381140dbb651d4bb2b7d7e40 |
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| Source note | uspto-grants-1982_12 |
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