돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486437생성일: 2026년 10월 24일

1-Bromo-3-chlorobenzene → 3-(3-Chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochloride

https://huagongshe.com/ko/reaction/486437

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-3-chlorobenzeneHCID 7928—
반응물TetrahydrofuranHCID 8028—
반응물3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
반응물MagnesiumHCID 5462224—
용매Acetic AcidHCID 176—
생성물3-(3-Chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochlorideHCID 1909558676%

반응 단계

To a stirred and refluxed Grignard complex previously prepared starting from a mixture of 4.2 parts of 1-bromo-3-chlorobenzene, 5.4 parts of magnesium and 135 parts of tetrahydrofuran were added dropwise 19 parts of 1-(phenylmethyl)-3-piperidinone. Upon completion, stirring was continued for 1 hour at reflux temperature. After cooling, the reaction mixture was poured into ice water and 12.5 parts of acetic acid. The layers were separated. The aqueous phase was extracted with trichloromethane. The organic layer was washed with water, dried, filtered and evaporated. The residue was converted into the hydrochloride salt in 2-propanol. The salt was filtered off and dried, yielding 26 parts (76%) of 3-(3-chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochloride (intermediate 27).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292738
출처 데이터셋uspto-grants-1994_03
ORD IDord-6aaafb2e7202497f9a681d221835f2e6
출처 메모uspto-grants-1994_03