Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Propanedioic acid, [(2,4-dichlorophenyl)methyl]-, diethyl ester | HCID 12206515 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 86679083 | HCID 86679083 | 48% |
Reaction Steps
To a stirred solution of 2-(2,4-dichloro-benzyl)-malonic acid diethyl ester (6.4 g; 20 mmol) in methanol (30 ml) under argon at 23° C., was added dropwise a solution of sodium methoxide 5.4 M in methanol (4.3 ml; 23 mmol), resulting in a small exothermic (25° C.) reaction. After addition the reaction mixture was cooled to 10° C. Isoamyl nitrite (3.2 ml; 22 mmol) was added dropwise to the cooled mixture (temperature kept below 15° C.). The mixture was stirred for 2 hours at 10° C. and 1 h at 23° C. 2 N hydrochloric acid (10 ml) was added to the mixture which was stirred at 23° C. for 30 min. The reaction mixture was then poured in brine (200 ml) and extracted with ethyl acetate (3×100 ml). Combined organics were dried over sodium sulfate and evaporated under reduced pressure to give the crude solid which was recrystallized at 5° C. from cyclohexane to afford 2.5 g (48% of theory) of 3-(2,4-dichloro-phenyl)-2-(hydroxyimino)-propionic acid methyl ester as a white powder (melting point: 97-100° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552049B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-2b751544e19642b19f886983958046b1 |
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| Source note | uspto-grants-2013_10 |
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