Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | {3-[2-Chloro-4-(trifluoromethyl)phenoxy]phenyl}acetyl chloride | HCID 13630154 | — |
| Product | HCID 13629660 | HCID 13629660 | — |
Reaction Steps
0.9 g of N,O-dimethylhydroxylamine and 1.5 g of triethylamine were dissolved in 20 ml of N,N-dimethylacetamide at 5° C., followed by addition of 3.5 g of 3-(2'-chloro-4'-trifluoromethylphenoxy)phenylacetyl chloride. The reaction was allowed to proceed at 5° C. for 1 hour and then at room temperature for further 3 hours to complete the reaction. After completion of the reaction, 50 ml of water was added to the liquid reaction mixture, followed by extraction twice with 30 ml portions of ether. The ether layer was washed with dilute hydrochloric acid and water and dried over anhydrous sodium sulfate, and the ether was distilled off under reduced pressure to obtain 3.5 g of N-methyl-N-methoxy-2-nitro-5-(2'-chloro-4'-trifluoromethylphenoxy)phenylacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04698094 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-9e363918f8204b4f89976ead429501ce |
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| Source note | uspto-grants-1987_10 |
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