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HRID 543519作成日:2026年10月27日

(3aR,4R,5R,6aS)-4-formyl-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate → (1S,5R,6R,7R)-7-Benzoyloxy-6-[(E)-(4RS) 4-methyl-3-oxonon-1-en-7-inyl]-2-oxabicyclo[3,3,0]octan-3-one

https://huagongshe.com/reaction/543519

反応式

関与物質

役割名称HCID仕込み量
反応物(3aR,4R,5R,6aS)-4-formyl-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoateHCID 11000244—
反応物3-Methyl-2-oxooct-6-inylphosphonic acid dimethyl esterHCID 53860064—
生成物(1S,5R,6R,7R)-7-Benzoyloxy-6-[(E)-(4RS) 4-methyl-3-oxonon-1-en-7-inyl]-2-oxabicyclo[3,3,0]octan-3-oneHCID 1865009985.8%

反応手順

Analogously to Example 1(g), 7.4 g of the title compound was synthesized from 5.4 g of 3-methyl-2-oxooct-6-inylphosphonic acid dimethyl ester and 6 g of (1S,5R,6R,7R)-6-formyl-7-benzoyloxy-2-oxabicyclo[3,3,0]-octan-3-one [E. J. Corey et al., J. Amer. Chem. Soc. 91: 5675 (1969)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04446147
出典データセットuspto-grants-1984_05
ORD IDord-463b5e102a7545b3bc5e852423f7c37e
出典メモuspto-grants-1984_05