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Water → 2-(4-Chlorophenoxymethyl)-2-(2,2-difluoro-1-methylcyclopropyl)-oxirane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Trimethylsulfonium methyl sulfate | HCID 2760871 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 1-(4-Chlorophenoxyacetyl)-1-methyl-2,2-difluorocyclopropane | HCID 14695240 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-(4-Chlorophenoxymethyl)-2-(2,2-difluoro-1-methylcyclopropyl)-oxirane | HCID 14695241 | — |
反応手順
2.4 g (0.044 mol) of sodium methoxide are added to the solution of 30 ml (0.04 mol) of a 1.36-molar solution of trimethylsulphonium methylsulphate in acetonitrile, and the mixture is stirred at room temperature for 30 minutes. 5.8 g (0.022 mol) of 1-(4-chlorophenoxyacetyl)-1-methyl-2,2-difluorocyclopropane are then added, and the mixture is stirred for 16 hours at 20° C. The reaction mixture is poured into 200 ml of water and extracted using methylene chloride, and the organic phase is washed with water and concentrated. 4.3 g (GC content of 73%; 71.6% of theory) of 2-(4-chlorophenoxymethyl)-2-(2,2-difluoro-1-methylcyclopropyl)-oxirane are obtained as a viscous resin which is reacted further directly. ##STR79##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05047415 |
| 出典データセット | uspto-grants-1991_09 |
| ORD ID | ord-8573277f0284485aa2b75c76d01aa420 |
| 出典メモ | uspto-grants-1991_09 |