Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 54443146 | HCID 54443146 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86757955 | HCID 86757955 | — |
Reaction Steps
A solution of 6.12 g of 1-(4-chlorophenyl)-propane-1,2-dione-1-(O-methyloxime) in 20 ml of ethanol is mixed with 4 ml of hydrazine hydrate. After stirring for 21 hours at room temperature, 80 ml of hexane are added. The precipitated crystals are filtered off, washed with a little hexane and dried. In this way, 4.5 g of 1-(4-chlorophenyl)-2-hydrazono-propan-1-one O-methyloxime are obtained as white crystals having a melting point of 118-119° C. A solution of 3.06 g of the above substance and 3.0 g of (2-formylphenyl)-methoxyimino-acetic acid methyl ester (EP 621277) in 30 ml of pyridine is stirred for 18 hours at 90° C. After cooling, the reaction solution is poured onto ice water and the precipitated oil is extracted with ethyl acetate. Purification takes place with ethyl acetate/hexane (1:9) on silica gel, and the title compound is obtained as a viscous, yellow oil, which crystallises after some time. (melting point 104-105° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372787B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-61de0fca87134e59a2ca8a355cfdf431 |
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| Source note | uspto-grants-2002_04 |
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