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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1669965생성일: 2026년 10월 24일

2,5-Dichloronitrobenzene → Escitalopram

https://huagongshe.com/ko/reaction/1669965

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DichloronitrobenzeneHCID 6977—
반응물Potassium CarbonateHCID 11430—
반응물Oxalic acid dihydrateHCID 61373—
반응물Citadiol, (S)-HCID 7472057—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물EscitalopramHCID 146570—
생성물Escitalopram OxalateHCID 146571—

반응 조건

온도102.5 °C

반응 단계

To a solution of 54.5 kg of (S)-(−)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)benzonitrile in 255 lit DMSO was added 66.0 kg of anhydrous K2CO3 and 36.7 kg of 2,5-dichloronitrobenzene at room temperature and stirred for 16 hours at 100-105° C. To the reaction mixture 2550 lit of water was added at about 30° C. The reaction mixture was 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 435 lit IPA at 30° C. and 17.7 kg of oxalic acid dihydrate was added to it, heated to 70-75° C., stirred and charcolized the clear solution, cooled, The filtrate was cooled to 5-10° C. slowly and the resultant solid was filtered, dried at 60° C. and micronised to get the oxalic acid salt of (S)-(+)-1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofuran carbonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989645B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-62710b81a2d74fc6bc3920cbd6f658f6
출처 메모uspto-grants-2011_08