HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411101Generated: October 25, 2026
1-Methylimidazole → n-Hexyl p-nitrophenyl phosphorochloridate
https://huagongshe.com/reaction/411101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Cetyl Alcohol | HCID 2682 | — |
| Reactant | Phosphorodichloridic acid, 4-nitrophenyl ester | HCID 69898 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | n-Hexyl p-nitrophenyl phosphorochloridate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06558657B1 |
|---|
| Source dataset | uspto-grants-2003_05 |
|---|
| ORD ID | ord-b3156d0f5b14489da27805f4034cda23 |
|---|
| Source note | uspto-grants-2003_05 |
|---|