돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270035생성일: 2026년 10월 27일

2-Bromo-4-fluoroanisole → Tert-butyl 4-(5-fluoro-2-methoxybenzyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/270035

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4-fluoroanisoleHCID 136292—
반응물tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
반응물HCID 178418918HCID 178418918—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(5-fluoro-2-methoxybenzyl)-4-hydroxypiperidine-1-carboxylateHCID 59833653—

반응 조건

온도20 °C

반응 단계

A solution of iso-propylmagnesium chloride in tetrahydrofuran (2M, 130 ml) was added dropwise over 30 minutes to a stirred solution of 2-bromo-4-fluoroanisole (34.2 ml) in anhydrous tetrahydrofuran (400 ml) at 30° C. under nitrogen. After a further 16 hours at 30° C., copper(I) bromide dimethyl sulphide complex (0.4 g) was added followed by a solution of 1-oxa-6-azaspiro[2.5]octane-6-carboxylic acid, 1,1-dimethylethyl ester (56.2 g) in anhydrous tetrahydrofuran (I 10 ml). After a further 3 hours at 30° C., the solution was cooled to 20° C., diluted with water (600 ml) and extracted with tert.-butyl methyl ether (600 ml) then ethyl acetate (600 ml). Combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure to give crude sub-title compound (86 g) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449475B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-f2ad4b7489a14157a1f0ce36e660c5c1
출처 메모uspto-grants-2008_11