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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500091Erstellt: 25. Oktober 2026

Sodium hydride → HCID 178453877, Verbindung

https://huagongshe.com/reaction/500091

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
EduktCyclopropyltriphenylphosphonium bromideHCID 2723931—
EduktHCID 178453955HCID 178453955—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178453877HCID 17845387743,1%

Reaktionsschritte

To a mixture of sodium hydride (1.06 g) and anhydrous tetrahydrofuran (50 ml) was added cyclopropyl-triphenylphosphonium bromide (10.13 g), the mixture was heated under reflux for 1 hour. The reaction mixture was cooled to ambient temperature, and then thereto was added a mixture of t-butyl trans-4-formylcyclohexylcarbamate (3.00 g), tris[2-(2-methoxyethoxy)ethyl]amine (427 mg) and anhydrous tetrahydrofuran (15 ml). The resulting mixture was heated under reflux for 1 hour. The reaction mixture was cooled to ambient temperature, and then saturated aqueous ammonium chloride was added to the reaction mixture. The reaction mixture was extracted with ethyl acetate, the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. The residue was purified by a silica gel chromatography (eluent: gradient from 100% hexane/0% ethyl acetate to 0% hexane/100% ethyl acetate) to give 1.43 g of t-butyl trans-4-cyclopropylidenemethylcyclohexylcarbamate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07767854B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-9270142efa654b0cbefa7320fe97f2c8
Quellennotizuspto-grants-2010_08