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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1639437생성일: 2026년 10월 26일

Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)- → (R)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylate

https://huagongshe.com/reaction/1639437

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)-HCID 156232—
반응물(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]cyclopropane-carboxylic acidHCID 86740318—
용매ChloroformHCID 6212—
생성물(R)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylateHCID 86740317—

반응 단계

Using the procedure of Step F of Example 9, (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylic acid and (R)α-cyano-3-phenoxy-benzyl alcohol were reacted to obtain (R)α-cyano-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20 =+117.5°±3° (c=0.6% in chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04883806
출처 데이터셋uspto-grants-1989_11
ORD IDord-9b15b657537a49da985c5ed4cdab7a5c
출처 메모uspto-grants-1989_11