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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275639생성일: 2026년 10월 24일

1-Methylimidazole → n-Hexyl p-nitrophenyl phosphorochloridate

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

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물Cetyl AlcoholHCID 2682—
반응물Phosphorodichloridic acid, 4-nitrophenyl esterHCID 69898—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물n-Hexyl p-nitrophenyl phosphorochloridateHCID 22501465—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352692B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-fe515c78279a4ae9b068ac47efdf3766
출처 메모uspto-grants-2002_03