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HRID 413932作成日:2026年10月25日

Tributylphosphine → (Z)-(S)-2-ethoxy-3-[4-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-phenyl]-propionic acid ethyl ester

https://huagongshe.com/reaction/413932

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
反応物Ethyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 9816147—
反応物(Z)-3-methyl-5-phenyl-pent-2-en-4-yn-1-olHCID 21597249—
溶媒BenzeneHCID 241—
生成物(Z)-(S)-2-ethoxy-3-[4-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-phenyl]-propionic acid ethyl esterHCID 86583976—

反応手順

1,1′-(azodicarbonyl) dipiperidine (0.504 g, 2.0 mmol) was added at 0° C. to a stirred solution of tributylphosphine (0.493 mL, 2.0 mmol), (Z)-3-methyl-5-phenyl-pent-2-en-4-yn-1-ol (0.172 g, 1.0 mmol) (J. Org. Chem. 1999, 64 (21), 7687-7692), and (S)-ethyl 2-ethoxy-3-(4-hydroxyphenyl)-propionate (0.262 g, 1.1 mmol) in dry benzene (20 mL), the mixture allowed to warm to room temperature, and stirring continued for 24 h. The resulting mixture was evaporated in vacuo, and the residue purified by flash column chromatography on silica gel (20% ethyl acetate in n-heptane eluent) to give (Z)-(S)-2-ethoxy-3-[4-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-phenyl]-propionic acid ethyl ester as an oil; 0.267 g (68%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06569901B2
出典データセットuspto-grants-2003_05
ORD IDord-887474af8a8c42a49519969c348508ee
出典メモuspto-grants-2003_05