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HRID 338825作成日:2026年10月27日

Trifluoroacetic acid → (R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one

https://huagongshe.com/reaction/338825

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
反応物(R)-3-methacryloyl-4-phenyloxazolidin-2-oneHCID 677330—
溶媒TolueneHCID 1140—
生成物(R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-oneHCID 70983198683.5%

反応手順

To a solution of (R)-3-methacryloyl-4-phenyloxazolidin-2-one (135.00 g, 583.79 mmol) and TFA (4.497 mL, 58.379 mmol) in dry toluene (50 mL) at <10° C. was quickly added dropwise N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)methanamine (194.16 mL, 758.93 mmol), and the mixture was stirred at ambient temperature overnight. The reaction was filtered and the filtrate was extracted with 4N HCl (3×250 mL). The aqueous layer was washed with ethyl acetate (250 mL) then made basic with solid K2CO3 to pH 10. The basic aqueous layer was extracted with ethyl acetate (4×400 mL), dried (MgSO4), filtered and concentrated under reduced pressure to provide (R)-3-((S)-1-benzyl-3-methylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one (145 g, 399 mmol, 68% yield) as a dark oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889704B2
出典データセットuspto-grants-2014_11
ORD IDord-02446b8d51614e65beb02f4f717ac37d
出典メモuspto-grants-2014_11