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HRID 13104作成日:2026年10月26日

Ethyl Acetate → (S)-tert-butyl 1-oxo-1-phenylpentan-2-ylcarbamate

https://huagongshe.com/reaction/13104

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Ammonium ChlorideHCID 25517—
反応物(S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopentan-2-ylcarbamateHCID 9992774—
反応物HCID 178418255HCID 178418255—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-tert-butyl 1-oxo-1-phenylpentan-2-ylcarbamateHCID 59339674—

反応手順

In a 50 mL round-bottomed flask was (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopentan-2-ylcarbamate (91d, 250 mg, 0.96 mmol) dissolved in THF (9.6 ml). Phenylmagnesium bromide (2.88 ml, 2.88 mmol) 1.0 M in THF was added. The reaction was stirred at r.t. for 5 h. The reaction was poured into a mixture of saturated ammonium chloride and ethyl acetate. The mixture was shaken and the layers separated. The water layer was washed twice with ethyl acetate. The combined organic layers were washed once with a small portion of water and dried over sodium sulphate. The solvent was evaporated and the crude product was purified by flash chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728030B2
出典データセットuspto-grants-2010_06
ORD IDord-1ba14a93921b47a5b43504fa8549e008
出典メモuspto-grants-2010_06