関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Chloro-3,5-dinitrobenzotrifluoride | HCID 9809 | — |
| 反応物 | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Benzenamine, N-methoxy-2,6-dinitro-4-(trifluoromethyl)- | HCID 12102672 | — |
反応手順
To a solution prepared from 27.0 g. (0.1 mole) of 4-chloro-3,5-dinitrobenzotrifluoride in 200 ml. of ethanol there was added 25.25 g. (0.25 mole) of triethylamine, and 12.5 g. (0.15 mole) of methoxyamine hydrochloride. Upon the addition of the methoxyamine hydrochloride, the temperature of the reaction mixture rose to about 50° C. The reaction mixture was allowed to stir for about 11/2 hours and the reaction product mixture was worked up by diluting with ethyl acetate, washing several times with dilute hydrochloric acid and water, and drying the organic layer over anhydrous magnesium sulfate. The drying agent was filtered off and the filtrate concentrated on the steam bath to leave a residue. The residue was allowed to chill over the weekend in the refrigerator and crystals separated. The crystalline product was filtered off. It had a melting point of about 135°-137° C., weighed 21.0 g., and was identified by NMR spectrum and elemental analyses as 2,6-dinitro-N-methoxy-α,α,α-trifluoro-p-toluidine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04087460 |
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| 出典データセット | uspto-grants-1978_05 |
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| ORD ID | ord-751c3818556047f8824abb978828dfb8 |
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| 出典メモ | uspto-grants-1978_05 |
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