Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5,6-Dichloronicotinic acid | HCID 247987 | — |
| Reactant | HCID 54284555 | HCID 54284555 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53635908 | HCID 53635908 | — |
Reaction Steps
Sodium hydride (60%, 0.15 g, 3.7 mmol) was added to a solution of 3-fluoro-2-hydroxymethyl-α-methyoxyimino-N-methyl-benzeneacetamide (0.54 g, 2.25 mmol) in dry THF (10 mL) and stirred for 10 minutes at 25° C. under N2 atmosphere. 5,6-Dichloronicotinic acid; t-butyl ester (0.59 g, 2.5 mmol) in 2-3 mL THF was added to this reaction mixture and stirred at 25° C. for about 2 hours. Water (40 mL) was added and the resulting mixture was extracted with ether (2×), dried (anhydrous Na2SO4), filtered and concentrated in vacuo to yield 1.2 g crude oil. Oil was chromatographed with dry pack silica gel (230-400 mesh) with descending solvent gradient from 100% petroleum ether to 80/20 pet ether/ethyl acetate as mobile phase. Elution and concentrated gave α-(methoxyimino)-N-methyl-2-[[[3-chloro-5-(t-butoxycarbonyl)-2-pyridinyl]oxy]methyl]-3-fluoro-benzeneacetamide (520 mg) as an oil. (98% E isomer; 2% Z isomer).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05968875 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-5c425fc3689446619db3f2a2fd963184 |
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| Source note | uspto-grants-1999_10 |
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