Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 28743252 | HCID 28743252 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 89103754 | HCID 89103754 | 84.8% |
Reaction Steps
2 ml of acetic acid and 0.64 g of iron(0) are added to 0.94 g of 1-[5-methyl-1-(4-nitrophenyl)-1H-pyrazol-4-yl]ethanone (Journal of Chemical Research, Synopses (1986), (5), 166-7) in 60 ml of EtOH/water mixture (65/35; v/v). It is heated at 75° C. for 2 hours. It is concentrated, filtered on Celite®, the filtrate is neutralized with saturated Na2CO3 and it is extracted with DCM. The organic phase is washed with water, with brine, it is dried over Na2SO4 and evaporated. 0.70 g of yellow powder is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623862B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-b0e117b8c9cd4172a4e1f1508147bd44 |
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| Source note | uspto-grants-2014_01 |
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