Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Glyoxylic Acid | HCID 760 | — |
| Reactant | HCID 22114846 | HCID 22114846 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22114835 | HCID 22114835 | 87% |
Reaction Steps
A mixture of 10.0 g of 2-(3,4-diaminophenyl)-3-chloro-5-trifluoromethylpyridine, 5.7 g of a 50% strength by weight aqueous glyoxalic acid solution, 100 ml of ethanol and 50 ml of glacial acetic acid was stirred at 23° C. for 2.5 hours. The solid portion formed was separated off, washed with ethanol and dried. After concentrating, the filtrate gave a further amount of the products. Total yield: 87% (9.9 g of colorless crystals); isomeric ratio according to 1H-NMR=about 1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06165941 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-34dd594c939b4da0a604b3df564cbbc0 |
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| Source note | uspto-grants-2000_12 |
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