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HRID 1388079作成日:2026年10月25日
(2,4-Dichlorophenoxy)acetyl chloride → 3-[(1-Ethylpropyl)amino]-6-methyl-2,4-dinitrobenzyl (2,4-dichlorophenoxy)acetate
https://huagongshe.com/reaction/1388079
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (2,4-Dichlorophenoxy)acetyl chloride | HCID 69887 | — |
| 反応物 | 3-((1-Ethylpropyl)amino)-6-methyl-2,4-dinitrobenzyl alcohol | HCID 156688 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 3-[(1-Ethylpropyl)amino]-6-methyl-2,4-dinitrobenzyl (2,4-dichlorophenoxy)acetate | HCID 12940764 | — |
反応手順
3-[(1-Ethylpropyl)amino]-6-methyl-2,4-dinitrobenzyl alcohol (2.0 g; 0.007 mol) and 2,4-dichlorophenoxyacetyl chloride (used in excess over theory) are dissolved in benzene, and the solution stirred at 60° C. until tlc (silica gel-benzene) indicates the reaction to be complete. The reaction mixture is then cooled down, diluted with ether, and washed with dilute sodium bicarbonate solution until the washings became alkaline. The organic layer is then separated, dried over magnesium sulfate, and evaporated to afford a liquid residue, which solidifies gradually (3.3 g; 94%). Recrystallization of this solid from methanol affords 1.4 g of title product, melting point 103°-106° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04430114 |
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| 出典データセット | uspto-grants-1984_02 |
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| ORD ID | ord-35a06acdc4b8426fbb81651fdf2f46c2 |
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| 出典メモ | uspto-grants-1984_02 |
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