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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1756953생성일: 2026년 10월 24일

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 54381600, 화합물

https://huagongshe.com/ko/reaction/1756953

반응식

참여 물질

역할이름HCID투입량
반응물1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
반응물Triphenylundecylphosphonium bromideHCID 3085198—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물HCID 54381600HCID 5438160064%

반응 단계

A solution of n-BuLi (4.1 mL, 6.5 mmol, 1.6M in hexanes) was added dropwise to a suspension of n-undecyl-triphenylphosphoniumbromide (3.09 g, 6.2 mmol, obtained from triphenylphosphine and undecylbromide) in 100 mL THF at -78° C. under an atmosphere of N2. The resulting orange solution was stirred for 45 minutes before a solution of 1-(triphenylmethyl)-4-imidazolecarboxaldehyde (2.0 g, 5.9 mmol, Ref: Kelly JL, Miller CA, and McLean EW, J. Med. Chem. 1977;20:721) in 75 mL THF was added dropwise. Warmed to room temperature and stirred for 16 hours. Quenched by adding 50 mL saturated NH4Cl solution and concentrating in vacuo. The residue was partitioned between water and dichloromethane. The organic layer was dried over MgSO4, filtered, and concentrated to give a yellow oil. Chromatography (10% EtOAc/hexanes on silica) gave the title compound (1.8 g, 64% ) as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05441975
출처 데이터셋uspto-grants-1995_08
ORD IDord-b05c7116fe4842f4b46bea5f2dd6778f
출처 메모uspto-grants-1995_08