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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349741생성일: 2026년 10월 25일

1,2-Dichloro-4-fluorobenzene → 4-(3,4-Dichlorophenoxy)-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/349741

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dichloro-4-fluorobenzeneHCID 74028—
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—
반응물Potassium tert-butoxideHCID 23665647—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물4-(3,4-Dichlorophenoxy)-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl esterHCID 11212544—

반응 단계

To a solution of potassium tert-butoxide (139.0 g, 1.24 mol) in THF (500 ml) was added a solution of the product of Step 1 (176.2 g, 0.62 mol) in THF (1000 ml). The reaction mixture was stirred 10 minutes before the additon of 3,4 dichlorofluorobenzene (122.8 g, 0.74 mol), this caused a green colouration that subsequently faded. The reaction mixture was then heated at reflux for 90 minutes. The reaction mixture was then cooled to room temperature before the addition of saturated NaHCO3 (1600 ml). The layers were separated and the organic layer stripped to leave an orange semi-solid. The solid was dissolved in DCM (1500 ml) and dried (MgSO4), filtered and the solvent removed. To the resultant solid was added methyl tert-butyl ether (MTBE) (54 ml) and iso-hexane (1000 ml) to give a slurry which was stirred overnight. The slurry was then filtered and washed with isohexane (200 ml) and the solid dried in vacuo at 50° C. to give the sub-titled compound as a pale powder, (211.6 g, 80%; MS: (M+H) 429).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179922B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-fa76b7452d9a43bf95ccd356985efa47
출처 메모uspto-grants-2007_02