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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55080생성일: 2026년 10월 24일

4-Nitrobenzenethiol → 2-[(4-Nitrophenyl)sulfanyl]-1H-benzimidazole

https://huagongshe.com/ko/reaction/55080

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrobenzenethiolHCID 15809—
반응물2-ChlorobenzimidazoleHCID 78572—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
용매EthanolHCID 702—
생성물2-[(4-Nitrophenyl)sulfanyl]-1H-benzimidazoleHCID 1261762515.3%

반응 단계

2-Chlorobenzimidazole (0.033 moles, 5.0 g), 4-nitrothiophenol (0.033 moles, 4.14 g), and DBU (0.033 moles, 5.0 g) in 200 ml ethanol were heated at 55° C. for 3 hr. The reaction was concentrated, ethyl acetate added, washed with water, dried over sodium sulfate and the solvent removed. The solid was slurred in hexane to yield 2-(4-nitrophenylthio)benzimidazole 1.37 g, 15%. Mass Spec (FD) 271. Calculated for C13H8N3O2S: C, 57.55; H, 3.34; N, 15.49. Found: C, 57.50; H, 5.54; N, 15.23.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624937
출처 데이터셋uspto-grants-1997_04
ORD IDord-e19f3c68bd474193823c5cefc616e6b8
출처 메모uspto-grants-1997_04