참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Methylimidazole | HCID 1390 | — |
| 반응물 | Cetyl Alcohol | HCID 2682 | — |
| 반응물 | Phosphorodichloridic acid, 4-nitrophenyl ester | HCID 69898 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | n-Hexyl p-nitrophenyl phosphorochloridate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06352692B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-fe515c78279a4ae9b068ac47efdf3766 |
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| 출처 메모 | uspto-grants-2002_03 |
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