Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 22125751 | HCID 22125751 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22125743 | HCID 22125743 | — |
Reaction Steps
Pyridine (16 ml) and concentrated hydrochloride acid (16.6 ml) were heated at 150° C. until the evaporation of water was ceased. 3-(2,6-Dinitro-3-hydroxy-4-methoxyphenyl)propanoic acid (2.3 g) was added and the resulting mixture heated at reflux for two minutes. The product mixture was cooled to about 150° C. and poured to ice water. The mixture was extracted with ethyl acetate and the product finally recrystallized from acetic acid. Yield: 0.93 g, melting point 165-166° C. NMR-data identical to that of example 11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150412 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-0efef2f26f434111a579d9790993aa4d |
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| Source note | uspto-grants-2000_11 |
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