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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275639Erstellt: 24. Oktober 2026

1-Methylimidazole → n-Hexyl p-nitrophenyl phosphorochloridate

https://huagongshe.com/de/reaction/275639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylimidazoleHCID 1390—
EduktCetyl AlcoholHCID 2682—
EduktPhosphorodichloridic acid, 4-nitrophenyl esterHCID 69898—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
Produktn-Hexyl p-nitrophenyl phosphorochloridateHCID 22501465—

Reaktionsschritte

p-Nitrophenyl phosphorodichloridate (75 g, 0.29 mol) in anhydrous dichloromethane (300 mL) was added to a 1 L, three necked, round-bottomed flask with stir bar that had been purged with N2. A solution of hexadecanol (71.03 g, 0.29 mol) and N-methylimidazole (23.35 mL, 0.29 mol) in anhydrous dichloromethane (250 mL) was added dropwise over a period of 2 hours. The reaction mixture was stirred for an additional 1 hour before pouring into a 1 L separatory funnel. N-methylimidazole hydrochloride salts separated at the bottom as an oil and were removed from the funnel. Dichloromethane was removed from the mixture at less than 30° C. under vacuum to give an amber oil which was taken up in hexane (400 mL) and placed in a freezer overnight. The reaction mixture was then thawed and the soluble portion was filtered to remove the crystals of p-nitrophenyl phosphorodichloridate. The solvent was removed from the filtrate via rotary evaporation at less than 35° C. to give n-hexyl p-nitrophenyl phosphorochloridate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352692B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-fe515c78279a4ae9b068ac47efdf3766
Quellennotizuspto-grants-2002_03