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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28753Erstellt: 24. Oktober 2026

Hexamethylphosphoramide → 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/de/reaction/28753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexamethylphosphoramideHCID 12679—
EduktCarbonocyanidic acid, methyl esterHCID 28660—
EduktLithium diisopropylamideHCID 2724682—
Edukt4-(2-Benzyloxyethyl)cyclohexanoneHCID 21879605—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl esterHCID 57443243—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of LDA (33 ml, 1.5 M in Et2O) in THF (50 mL) at −78° C. was treated with 4-(2-benzyloxy-ethyl)-cyclohexanone (9.5 g, 40.2 mmol). The mixture was warmed to 0° C. over 30 m before re-cooling to −78° C. and adding HMPA (7 mL). Methyl cyanoformate (4.1 mL, 85 mmol) was added and the mixture was stirred for 15 m before aqueous quench and work-up. The product was purified by chromatography on SiO2 with 10% EtOAc:Hx. 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester was isolated, 5.8 g (49%) and reduced with an equivalent of NaBH4 in MeOH at −10° C. to provide the alcohol (Intermediate R2). Intermediate R2 was purified by chromatography on SiO2 with 30 to 50% EtOAC:Hx. (˜90% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419994B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-b7058c7b568a446c9a7a2baaab627763
Quellennotizuspto-grants-2008_09