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HRID 1756949作成日:2026年10月24日

Triphenylundecylphosphonium bromide → HCID 54242059、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenylundecylphosphonium bromideHCID 3085198—
反応物ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetateHCID 10563150—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 54242059HCID 54242059—

反応手順

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%).

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-c4de1ad2990442318a9ae27313a6992b
出典メモuspto-grants-1995_08