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HRID 569528作成日:2026年10月27日

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/569528

反応式

関与物質

役割名称HCID仕込み量
反応物Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)-HCID 156232—
反応物(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]cyclopropane-carboxylic acidHCID 86740318—
溶媒ChloroformHCID 6212—
生成物(R)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylateHCID 86740317—

反応手順

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).

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-f8691d46e87b4c4eb87a915cb6409b11
出典メモuspto-grants-1988_03