戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1076962作成日:2026年10月25日

Triethyl ethane-1,1,2-tricarboxylate → Dimethyl trans-1-(Carboethoxymethyl)-5-(3-hydroxy-3-methyl-1-octenyl)-2-oxo-1,3-cyclopentanedicarboxylate

https://huagongshe.com/reaction/1076962

反応式

関与物質

役割名称HCID仕込み量
反応物Triethyl ethane-1,1,2-tricarboxylateHCID 81961—
反応物Sodium MethoxideHCID 10942334—
反応物Dimethyl trans-(3-methyl-3-hydroxy-1-octenyl)cyclopropane-1-1-dicarboxylateHCID 21328875—
溶媒MethanolHCID 887—
生成物Dimethyl trans-1-(Carboethoxymethyl)-5-(3-hydroxy-3-methyl-1-octenyl)-2-oxo-1,3-cyclopentanedicarboxylateHCID 70601158—

反応手順

To a solution of triethyl 1,1,2-ethanetricarboxylate (1.36 g) in 3 ml of methanol, a freshly prepared solution of sodium methoxide (from 0.126 g of sodium and 6 ml of absolute methanol) is added. The mixture is heated to 80°. A solution of dimethyl trans-(3-methyl-3-hydroxy-1-octenyl)cyclopropane-1-1-dicarboxylate (1.7 g) is gradually added and the resulting mixture stirred for an additional 15 min. The methanol is removed by distillation at reduced pressure. The residue is then heated at 100° for 45 min. Thereafter the mixture is cooled in an ice bath and rendered neutral with acetic acid. The mixture is extracted with ether. The extract is dried (Na2SO4) and concentrated. Chromatography of the residue on silica gel using ethyl acetate-benzene (1:4) as eluant gives the title compound, νmaxfilm 3350, 1727 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03959263
出典データセットuspto-grants-1976_05
ORD IDord-5c0170270acb49619fa01ed57c194229
出典メモuspto-grants-1976_05