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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1669962생성일: 2026년 10월 25일

2,5-Dichloronitrobenzene → Escitalopram Oxalate

https://huagongshe.com/reaction/1669962

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DichloronitrobenzeneHCID 6977—
반응물Potassium CarbonateHCID 11430—
반응물Oxalic acid dihydrateHCID 61373—
반응물Citadiol, (S)-HCID 7472057—
용매AcetoneHCID 180—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물Escitalopram OxalateHCID 146571—

반응 조건

온도100 °C

반응 단계

To a solution of 6.0 gm of (S)-(−)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)benzonitrile in 30 ml of DMSO at room temperature was added 7.3 gm of anhydrous K2CO3 and 4.04 gm of 2,5-dichloronitrobenzene was added to the above reaction mixture at room temperature and stirred at 100° C. for 15.0 hours. To the above reaction mixture, 120 ml of water was added, and extracted with toluene. The toluene layer was washed with water and 5% sodium hydroxide solution and after acid base treatment yielded an oily product. The oil was dissolved in 16 ml of acetone at 30° C. and 1.9 gm of oxalic acid dihydrate in 8 ml of acetone was added to it, stirred, cooled, filtered and dried at 60° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989645B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-7a213609d29543c4811ac4e2a999e69c
출처 메모uspto-grants-2011_08