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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 464458생성일: 2026년 10월 24일

(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrile → (S)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[Z-2-(cyclohexyloxycarbonyl)-ethenyl]-cyclopropane-carboxylate

https://huagongshe.com/ko/reaction/464458

반응식

참여 물질

역할이름HCID투입량
반응물(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrileHCID 9837437—
반응물(1R,cis)2,2-dimethyl-3-[Z-2-(cyclohexyloxycarbonyl)ethenyl]-cyclopropane-carboxylic acidHCID 70476826—
생성물(S)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[Z-2-(cyclohexyloxycarbonyl)-ethenyl]-cyclopropane-carboxylateHCID 8673900542.4%

반응 단계

Using the procedure of Step D in Example 7, 2.5 g of the product of Step C and 2.2 g of (S)α-cyano-3-phenoxybenzyl alcohol were reacted and the product was chromatographed over silica gel. Elution with a 9-1 hexane-ether mixture yielded 1.883 g of (S)α-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[Z-2-(cyclohexyloxycarbonyl)-ethenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20 =+41°±2.5° (c=0.5% in chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04547522
출처 데이터셋uspto-grants-1985_10
ORD IDord-0e0628f4a91e45858afbcc5d5c9d6b1e
출처 메모uspto-grants-1985_10