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HRID 569519作成日:2026年10月27日
Acetyl chloride → (RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-oxo-3-methoxymethoxy-1propynyl)-cyclopropane-carboxylate
https://huagongshe.com/reaction/569519
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetyl chloride | HCID 6367 | — |
| 反応物 | Dimethoxymethane | HCID 8020 | — |
| 反応物 | Bis(Chloromethyl) Ether | HCID 10967 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Monosodium phosphate | HCID 23672064 | — |
| 反応物 | (RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-hydroxy-3-oxo-1-propynyl)-cyclopropane-carboxylate | HCID 53972231 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-oxo-3-methoxymethoxy-1propynyl)-cyclopropane-carboxylate | HCID 54503448 | — |
反応手順
A solution of 3 g of (RS)α-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-hydroxy-3-oxo-1-propynyl)-cyclopropane-carboxylate in 30 ml of anhydrous dimethylformamide was cooled to +10° C. and 300 mg of 61% sodium hydride in oil were added in portions thereto. Then, over 15 minutes, 2.5 ml of chloromethyl ether solution prepared by mixing 4.5 ml of methylal and 0.52 ml of methanol and slowly adding 3.53 ml of acetyl chloride after which the mixture was stirred for 36 hours at room temperature. The mixture was stirred for 2 hours and was then poured into an aqueous solution of monosodium phosphate. The mixture was extracted with ethyl acetate and the organic phase was washed with water, dried and evaporated to dryness. The residue was chromatographed over silica gel and eluted with a 75-25 mixture of cyclohexane-ethyl acetate to obtain 2 g of (RS)α-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-oxo-3-methoxymethoxy-1propynyl)-cyclopropane-carboxylate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04732903 |
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| 出典データセット | uspto-grants-1988_03 |
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| ORD ID | ord-6993c52a9709414f9a845b75bea54f55 |
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| 出典メモ | uspto-grants-1988_03 |
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