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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2074458생성일: 2026년 10월 26일

Phosphorus pentachloride → HCID 178466243, 화합물

https://huagongshe.com/reaction/2074458

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus pentachlorideHCID 24819—
반응물N-(2-Amino-5-nitro-phenyl)-2-(4-ethoxy-phenyl)-acetamideHCID 59799754—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매Ammonium HydroxideHCID 14923—
생성물HCID 178466243HCID 178466243—

반응 단계

N-(2-Amino-5-nitro-phenyl)-2-(4-ethoxy-phenyl)-acetamide 41 (590 mg, 1.871 mmol), Phosphorous pentachloride (390 mg, 1.871 mmol) were dissolved in anhydrous chloroform (20 mL) in a small, argon purged flask fitted with an condenser and magnetic stirbar. The solution was heated to reflux in an oil bath for 4 hours and cooled to room temperature overnight. The mixture was diluted with H2O and chloroform and 2M ammonium hydroxide solution added to adjust pH to 9-10. The mixture was transferred to a separatory funnel and the organic layer collected. The aqueous layer was further extracted with chloroform and the combined organic layers were washed with brine, dried over magnesium sulphate, filtered and concentrated to afford crude. The product was purified using dry silica gel column chromatography eluting with 20 mL portions of solvent system (2.5% 2M NH3 in methanol/95% dichloromethane) to afford a yellow residue 42 2-(4-Ethoxy-benzyl)-5-nitro-1H-benzimidazole. 1H NMR (DMSO) δ: 1.30 (t, 3H, J=6.5), 3.87 (q, 2H, J=7.3), 4.11 (s, 2H), 6.88 (d, 2H, J=8.0), 7.25 (d, 2H, J=7.9), 7.65 (d, 1H, J=8.9), 8.07 (d, 1H, J=9.0), 8.36-8.40 (m, 1H); MS (ESI): 298 (MH+, 100%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07919510B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-a2b153bcfa3a4c59a9c0c9974527216f
출처 메모uspto-grants-2011_04