Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Cresol | HCID 335 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 54349771 | HCID 54349771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86751970 | HCID 86751970 | — |
Reaction Steps
A solution of 1.84 g of o-cresol in 15 ml of dimethylformamide is added dropwise at 20° C. to a suspension of 0.4 g of sodium hydride in 5 ml of dimethylformamide. After 3 hours a solution of 5.0 g of 2-(bromomethyl)-phenylglyoxalic acid methyl ester O-fluoromethyl oxime in 25 ml of dimethylformamide is added dropwise to the brown suspension. After 16 hours 0.3 g of thiourea is added thereto and the reaction mixture is heated at 30° C. for 0.5 hour. The reaction mixture is then poured onto a saturated sodium chloride solution and extraction is carried out with ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate, filtered and concentrated by evaporation. Chromatography on silica gel with hexane/ethyl acetate (9:1) yields pure 2-(2-methylphenoxymethyl)-phenylglyoxalic acid methyl ester O-fluoromethyl oxime; m.p. 101°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710314 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-0cc465395b6a4be78dd105532c2500a0 |
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| Source note | uspto-grants-1998_01 |
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