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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251394생성일: 2026년 10월 26일

Toluene → 4-[2-(2-Hydroxy-ethoxy)ethyl-piperazin-1-yl}-(2-iodophenyl)-methanone

https://huagongshe.com/reaction/251394

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물2-Iodobenzoic acidHCID 6941—
반응물TetrahydrofuranHCID 8028—
반응물Thionyl ChlorideHCID 24386—
반응물1-[2-(2-Hydroxyethoxy)ethyl]piperazineHCID 139436—
용매WaterHCID 962—
용매TriethylamineHCID 8471—
생성물4-[2-(2-Hydroxy-ethoxy)ethyl-piperazin-1-yl}-(2-iodophenyl)-methanoneHCID 86612490—

반응 단계

2-iodobenzoic acid (20 g, 0.081 mol), toluene (20 ml) and thionyl chloride (30 ml, 0.41 mol) were charged into a reaction flask. The mixture was stirred and refluxed for 11 h. Toluene (40 ml) was added and the solvent and excess of thionylchloride were distilled off under reduced pressure. The process was repeated with 20 ml of toluene. The residue of 2-iodobenzoyl chloride was dissolved into THF (20 ml). 1-[2-(hydroxyethoxy)-ethyl]-piperazine (14.1 g, 0.081 mol), THF (100 ml), water (50 ml) and triethylamine (12.3 ml) were added into a reaction flask and stirred at icewater bath temperature. The previously prepared 2-iodobenzoyl chloride THF solution was slowly added to the reaction mixture. The temperature was kept below 20° C. during the addition. The reaction mixture was allowed to warm to room temperature and stirred 2 h at ambient temperature. 50 ml of water was added and THF was removed by distillation. The pH of the solution was checked and adjusted to 9-10. The water was extracted three times with dichloromethane (50 ml). The combined organic phase was evaporated yielding {4-[2-(2-hydroxy-ethoxy)ethyl-piperazin-1-yl}-(2-iodophenyl)-methanone as a yellowish oil, which was used without further purification. Yield 31 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863441B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-d10ecaf510324ca9b05cc64ee8fd0311
출처 메모uspto-grants-2011_01