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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 860783생성일: 2026년 10월 26일

Sodium borohydride → 2-Amino-alpha-(3-chlorophenyl)-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]-benzenemethanol

https://huagongshe.com/reaction/860783

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물[2-Amino-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]phenyl](3-chlorophenyl)methanoneHCID 22626605—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-alpha-(3-chlorophenyl)-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]-benzenemethanolHCID 69019808100%

반응 단계

A mixture of [2-amino-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]phenyl](3-chlorophenyl)methanone (prepared as described in WO 98/49157) (0.088 mol) in methanol (300 ml) and THF (100 ml) was cooled on an ice bath. sodium tetrahydroborate (0.088 mol) was added portionwise. The mixture was stirred at a low temperature for 30 min, then hydrolized and extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated till dryness. The product was used without further purification, yielding 36.6 g (100%) of 2-amino-α-(3-chlorophenyl)-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]-benzenemethanol (intermediate 9).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07153958B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-233094ed9755435cbac414678207f1cd
출처 메모uspto-grants-2006_12