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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1408939Erstellt: 24. Oktober 2026

Diethyl Ether → HCID 59281702, Verbindung

https://huagongshe.com/de/reaction/1408939

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktCerium(III) chlorideHCID 24636—
Edukttert-butyl N-(2-oxocyclopentyl)carbamateHCID 357962—
EduktHCID 178418348HCID 178418348—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59281702HCID 5928170282%

Reaktionsschritte

A 1.6 M ether solution of methyllithium (13.59 mL, 21.75 mmol) was added to a stirred suspension of tert-butyl 2-oxocyclopentylcarbamate (1.97 g, 9.89 mmol, from Step 2) and cerium(III) chloride (5.36 g, 21.75 mmol) in tetrahydrofuran (50 mL) at −78° C. under nitrogen. After 2.5 h at −78° C., the mixture was quenched with saturated ammonium chloride, allowed to warm to room temperature, and filtered through a short bed of Celite to remove insoluble cerium salt. The filter cake was rinsed with ethyl acetate. The filtrated was extracted with ethyl acetate three times. The combined ethyl acetate phase was washed with saturated ammonium chloride and brine respectively, dried (MgSO4), filtered and concentrated. Silica gel chromatography, eluting with 0 to 50% ethyl acetate in hexanes, gave tert-butyl 2-hydroxy-2-methylcyclopentylcarbamate as yellow solid (1.47 g, 82% yield). 1H NMR analysis indicated the presence of approximately a 3:1 diastereomeric mixture.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08921368B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-8036fafc7a4e4e8e842ad322318190fa
Quellennotizuspto-grants-2014_12