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HRID 1581114Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1581114

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiazomethaneHCID 9550—
EduktMethyl 7-[2-hydroxy-5-(3-hydroxy-1-octenyl)cyclopentyl]heptanoateHCID 54187079—
EduktHCID 178494437HCID 178494437—
LösungsmittelDiethyl EtherHCID 3283—
ProduktMethyl 7-[2-methoxy-5-(3-methoxy-1-octenyl)cyclopentyl]heptanoateHCID 5411213665%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03935261
Quelldatensatzuspto-grants-1976_01
ORD IDord-684100cd70f9448aa516bdda328325d2
Quellennotizuspto-grants-1976_01