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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500070Erstellt: 24. Oktober 2026

Dimethylformamide → HCID 86629083, Verbindung

https://huagongshe.com/de/reaction/500070

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktAmmonium ChlorideHCID 25517—
Edukttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorButyltriphenylphosphonium bromideHCID 159628—
ProduktHCID 86629083HCID 86629083—

Reaktionsschritte

To a mixture of potassium t-butoxide (2.05 g) and anhydrous N,N-dimethylformamide (60 ml) was added butyltriphenylphosphonium bromide (7.30 g) at room temperature. The mixture was stirred for 15 minutes and then a solution of t-butyl 4-oxocyclohexylcarbamate (1.30 g) in N,N-dimethylformamide (10 ml) was added to the mixture. The reaction mixture was stirred at room temperature overnight and then saturated aqueous ammonium chloride was added to the mixture. The mixture was extracted with toluene, and the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. After diethyl ether was added to the residue, the precipitate was filtered off and then the filtrate was concentrated under reduced pressure. 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 1.40 g of t-butyl (4-butylidenecyclohexyl)carbamate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07767854B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-1fa0f1a583cb4d2886f66a95cb1ac0bd
Quellennotizuspto-grants-2010_08