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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569519생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물DimethoxymethaneHCID 8020—
반응물Bis(Chloromethyl) EtherHCID 10967—
반응물Sodium hydrideHCID 24758—
반응물Monosodium phosphateHCID 23672064—
반응물(RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-hydroxy-3-oxo-1-propynyl)-cyclopropane-carboxylateHCID 53972231—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물(RS)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-(3-oxo-3-methoxymethoxy-1propynyl)-cyclopropane-carboxylateHCID 54503448—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04732903
출처 데이터셋uspto-grants-1988_03
ORD IDord-6993c52a9709414f9a845b75bea54f55
출처 메모uspto-grants-1988_03