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HRID 660559作成日:2026年10月24日

3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)- → HCID 68839236、化合物

https://huagongshe.com/ja/reaction/660559

反応式

関与物質

役割名称HCID仕込み量
反応物3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 179824—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物{[2-(Ethoxycarbonyl)phenyl]methyl}(triphenyl)phosphanium bromideHCID 19092713—
溶媒TolueneHCID 1140—
生成物HCID 68839236HCID 68839236—

反応手順

To a suspension of (2-ethoxycarbonylbenzyl)-triphenylphosphonium bromide (9.0 g, 17.77 mmol) in toluene (100 mL) is added potassium bis(trimethylsilyl)amide (0.5M in toluene, 40 mL) followed by the addition of (S)-4-formyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester (3.4 g, 14.83 mmol) and the mixture is refluxed for 1 h. After cooling to RT, ice/water is added and the solution extracted with EtOAc. The organic layer is washed with brine, dried over MgSO4, filtered and concentrated. The crude material is purified by column chromatography to afford the title compound as a yellow oil: (M+1)+=376.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08084448B2
出典データセットuspto-grants-2011_12
ORD IDord-4796e25e8e5a4414b94bcacc3d4b7926
出典メモuspto-grants-2011_12