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HRID 1756953作成日:2026年10月24日

1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 54381600、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
反応物Triphenylundecylphosphonium bromideHCID 3085198—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 54381600HCID 5438160064%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05441975
出典データセットuspto-grants-1995_08
ORD IDord-b05c7116fe4842f4b46bea5f2dd6778f
出典メモuspto-grants-1995_08