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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1756949생성일: 2026년 10월 24일

Triphenylundecylphosphonium bromide → HCID 54242059, 화합물

https://huagongshe.com/ko/reaction/1756949

반응식

참여 물질

역할이름HCID투입량
반응물Triphenylundecylphosphonium bromideHCID 3085198—
반응물ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetateHCID 10563150—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물HCID 54242059HCID 54242059—

반응 단계

A solution of n-BuLi (127 mL, 254 mmol, 2.0M in hexanes) was added dropwise to a suspension of n-undecyl-triphenylphosphonium bromide (121.6 g, 244 mmol, obtained from triphenylphosphine and undecylbromide) in 500 mL THF at -78° C. under an atmosphere of N2. The resulting orange solution was stirred for 1 hour before a solution of ethyl (±)-4-formyl-α-phenyl-1H-pyrazole-1-acetate in 250 mL THF was added dropwise. Warmed to room temperature and stirred for 16 hours. Quenched by adding 150 mL water and concentrating in vacuo. The residue was partitioned between water and dichloromethane. The organic layer was dried over MgSO4, filtered, and concentrated to give an oily tan solid. Triturated with boiling hexanes and filtered to remove triphenylphosphine oxide. The filtrate was concentrated and chromatographed (10% EtOAc/hexanes on silica) to give the title compound as a yellow oil, a 1:2 E/Z mixture (44.4 g, 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05441975
출처 데이터셋uspto-grants-1995_08
ORD IDord-c4de1ad2990442318a9ae27313a6992b
출처 메모uspto-grants-1995_08