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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1393712생성일: 2026년 10월 27일

Tetrahydrofuran → Sertraline

https://huagongshe.com/reaction/1393712

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물N-(4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene)methanamineHCID 9796475—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
용매1,2-DichlorobenzeneHCID 7239—
생성물SertralineHCID 686170.75%

반응 단계

N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)naphthalenylidene]methanamine (Ketimine) (50 g), tetrahydrofuran (300 ml), Raney Nickel (0.15 g wet basis) and o-dichlorobenzene (25 ml) are charged into a reaction vessel. The mixture is hydrogenated at 5 to 6 kg/cm2 over pressure of hydrogen for 6 to 7 hrs at about 28 to 30° C. The catalyst is removed by filtration and the cake is washed with 50 ml tetrahydrofuran. The cis to trans ratio is 85 to 87/15 to 13. The amount of dehalogenated byproduct is <0.1%. Sertraline racemate free base thus formed is treated with hydrochloric acid (24 ml, 33%) and predominantly isomer of sertraline HCl racemate is filtered [Cis>95%, trans<5%, dehalogenation product<0.1%, yield 0.75 to 0.78%].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07345201B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-9fcdcd7fac214998aa0e8b122a38aade
출처 메모uspto-grants-2008_03