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HRID 1581114作成日:2026年10月27日

Diazomethane → Methyl 7-[2-methoxy-5-(3-methoxy-1-octenyl)cyclopentyl]heptanoate

https://huagongshe.com/reaction/1581114

反応式

関与物質

役割名称HCID仕込み量
反応物DiazomethaneHCID 9550—
反応物Methyl 7-[2-hydroxy-5-(3-hydroxy-1-octenyl)cyclopentyl]heptanoateHCID 54187079—
反応物HCID 178494437HCID 178494437—
溶媒Diethyl EtherHCID 3283—
生成物Methyl 7-[2-methoxy-5-(3-methoxy-1-octenyl)cyclopentyl]heptanoateHCID 5411213665%

反応条件

温度-40 °C

反応手順

A solution of methyl 7-[2-hydroxy-5-(3-hydroxy-1-octenyl)cyclopentyl]heptanoate (0.6 g.) [prepared as described in Example 5] in dry diethyl ether (30 ml.) was cooled to -40°C. Freshly prepared dry diazomethane in diethyl ether, cooled to -40°C., was added to the solution of methyl ester immediately after the addition of boron trifluoride dimethyl etherate (3 ml.). Diazomethane solution was added until the yellow colour persisted. After 15 minutes at -40°C. and standing at ambient temperature overnight the solution was filtered from precipitated polymethylenes, washed with sodium bicarbonate solution and water, dried over anhydrous sodium sulphate and evaporated in vacuo. The last traces of solvent were removed by pumping under high vacuum to give methyl 7-[2-methoxy-5-(3-methoxy-1-octenyl)cyclopentyl]heptanoate (0.42 g., 65%). (Found: C, 72.4; H, 10.3. C23H42O4 requires C, 72.3; H,11.0%) νmax 1730 cm-1, 1100 cm-1 and 990 cm-1 (liquid film).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03935261
出典データセットuspto-grants-1976_01
ORD IDord-684100cd70f9448aa516bdda328325d2
出典メモuspto-grants-1976_01