Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1159464Erstellt: 26. Oktober 2026

(Iodomethyl)cyclopentane → Methyl 3-cyclopentyl-2-(4-methylsulfonylphenyl)propionate

https://huagongshe.com/reaction/1159464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Iodomethyl)cyclopentaneHCID 2762531—
EduktMethyl 2-(4-(methylsulfonyl)phenyl)acetateHCID 16640928—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelMethidathionHCID 13709—
ProduktMethyl 3-cyclopentyl-2-(4-methylsulfonylphenyl)propionateHCID 19261331—

Reaktionsschritte

To a solution of diispropylamine (25 mmol, 3.6 mL) in 24 mL of THF and 7.5 mL of methidathion (DMTP) at −78° C. is added n-BuLi (25 mmol, 10 mL, 2.5 M in hexanes) and the mixture stirred for 15 min. 4-Methylsulfonylphenylacetic acid methyl ester (24 mmol, 5.47 g) in 24 mL of THF and 7.5 mL of DMTP is then added dropwise over 30 min and the reaction is stirred for 90 min further. Cyclopentylmethyliodide (28.9 mmol, 6.08 g) in 10 mL of THF is then added dropwise and the reaction is stirred for 1 h at −78° C. before allowing to warm to RT. After 12 h, the reaction is quenched with water, evaporated and then partitioned between ethyl acetate (EtOAc) and brine, and the organic solution is dried and evaporated to afford an oil. The crude material is chromatographed on silica (eluent: 5%→25% EtOAc in hexanes) to afford 3-cyclopentyl-2-(4-methanesulfonyl-phenyl)-propionic acid methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07812167B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-d8ef0e9e40c04f8c93c5fde6d48cf5da
Quellennotizuspto-grants-2010_10