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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5257Erstellt: 25. Oktober 2026

Water → 10-(4-Chlorophenyl)-dec-9-enoic acid methyl ester

https://huagongshe.com/reaction/5257

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl 9-oxononanoateHCID 74732—
Edukt(4-Chlorobenzyl)triphenylphosphonium chlorideHCID 2733546—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt10-(4-Chlorophenyl)-dec-9-enoic acid methyl esterHCID 5408894013%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 18.2 g (43 mmol) of 4-chlorobenzyltriphenylphosphonium chloride in 200 mL of dry tetrahydrofuran at -78° C. is added dropwise, 30.7 mL (43 mmol) of a 1.4M solution of potassium hexamethyldisilazide in tetrahydrofuran. This is allowed to stir for 1 hour when 8.0 g (43 mmol) of 8-carbomethoxyoctanal is added dropwise. The solution is stirred at -78° C. for 2 hours, allowed to warm to room temperature, and stirred for 2 days. The reaction is worked up by adding water and extracting three times with diethyl ether. The ether extracts are combined, washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give a yellow solid. Pad filtration through flash silica gel eluting with 10% ethyl acetate/hexane, gives a yellow oil after concentration in vacuo. Flash chromatography on a 60 mm×150 mm silica column eluting with 5% ethyl acetate/hexane gives 1.62 g (13%) of 10-(4-chlorophenyl)-dec-9-enoic acid methyl ester as a mixture of E and Z isomers.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05242945
Quelldatensatzuspto-grants-1993_09
ORD IDord-272149112272419dac09db7b59175fc6
Quellennotizuspto-grants-1993_09