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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

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物DimethoxymethaneHCID 8020—
反応物Bis(Chloromethyl) EtherHCID 10967—
反応物Sodium hydrideHCID 24758—
反応物Monosodium phosphateHCID 23672064—
反応物(RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-hydroxy-3-oxo-1-propynyl)-cyclopropane-carboxylateHCID 53972231—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物(RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-oxo-3-methoxymethoxy-1propynyl)-cyclopropane-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04732903
出典データセットuspto-grants-1988_03
ORD IDord-6993c52a9709414f9a845b75bea54f55
出典メモuspto-grants-1988_03