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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1770906생성일: 2026년 10월 26일

Tetrahydrofuran → 6'-Bromospiro[cyclopropane-1,2'-inden]-1'(3'H)-one

https://huagongshe.com/reaction/1770906

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1-(4-Bromo-2-iodobenzyl)cyclopropanecarbonitrileHCID 67979304—
반응물ButyllithiumHCID 178418339—
생성물6'-Bromospiro[cyclopropane-1,2'-inden]-1'(3'H)-oneHCID 6797945651%

반응 조건

온도-78 °C

반응 단계

A dried flask was charged with 1-(4-bromo-2-iodobenzyl)cyclopropanecarbonitrile (Intermediate 51, 3.29 g, 9.09 mmol) and dry THF (30 mL) was added under argon atmosphere. The resulting mixture was cooled to −78° C. and n-BuLi (2.5 M in hexanes, 7.27 mL, 18.2 mmol) was added dropwise. The solution was allowed to reach r.t. The reaction was quenched with MeOH (2 mL) and HCl (1M, 5 mL). The mixture was extracted with EtOAc. The water phase was basified with sat NaHCO3 and extracted with EtOAc twice. The organic phases were combined, dried over MgSO4, filtered and concentrated in vacuo. HCl (1 M, 4 mL) and DCM (5 mL) were added and the organic phase was collected. This was repeated twice. The water phase was basified with sat NaHCO3 and extracted with DCM. The combined organic phases were dried through a phase separator and evaporated to dryness to give the title compound (1.1 g, 51% yield): MS (CI) m/z 237 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09248129B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-de6d00509f8c46b8a61332a2dc440fe2
출처 메모uspto-grants-2016_02