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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368007Generated: October 25, 2026

1-Methylimidazole → n-Hexyl p-nitrophenyl phosphorochloridate

https://huagongshe.com/reaction/1368007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantCetyl AlcoholHCID 2682—
ReactantPhosphorodichloridic acid, 4-nitrophenyl esterHCID 69898—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Productn-Hexyl p-nitrophenyl phosphorochloridateHCID 22501465—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06572850B1
Source datasetuspto-grants-2003_06
ORD IDord-47d5c7ac64c44890acbc43a75c0890a8
Source noteuspto-grants-2003_06