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HRID 1039729作成日:2026年10月26日

Imidazole → Tributylphosphine oxide

https://huagongshe.com/reaction/1039729

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物TributylphosphineHCID 13831—
反応物Sodium hydrideHCID 24758—
反応物(S)-tert-butyl 2-((S)-1,2-bis(tert-butyldimethylsilyloxy)ethyl)aziridine-1-carboxylateHCID 86635713—
溶媒TolueneHCID 1140—
生成物Tributylphosphine oxideHCID 13138—
生成物tert-butyl (2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(1H-imidazol-1-yl)butan-2-ylcarbamateHCID 57950888—

反応手順

A solution of (5)-tert-butyl 2-((S)-1,2-bis(tert-butyldimethylsilyloxy)ethyl)aziridine-1-carboxylate (0.740 g, 1.7 mmol) and 1H-imidazole (0.35 g, 5.1 mmol) in 3 mL toluen was thoroughly degassed and treated with tributylphosphine (0.42 ml, 1.7 mmol). The reaction mixture was heated to reflux and allowed to stir for 3 hours. NaH (60% dispersion in mineral oil) (0.069 g, 2.9 mmol) was added and the reaction mixture was allowed to stir at 110° C. overnight. The reaction mixture was quenched with saturated NH4Cl solution and diluted with EtOAc. The reaction mixture was washed with water then brine. The organics were dried over MgSO4 and concentrated in vacuo. Purification of the crude residue by column chromatography gave tert-butyl (2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(1H-imidazol-1-yl)butan-2-ylcarbamate with tributylphosphine oxide as the major impurity. This material was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552181B2
出典データセットuspto-grants-2013_10
ORD IDord-fca6ca29bd5b4a0cb7261eb70aaef559
出典メモuspto-grants-2013_10