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HRID 1021063作成日:2026年10月27日

Chloride → 1-Benzyl-5-biphenyl-4-ylmethyl-5-hydroxy-pyrrolidin-2-one

https://huagongshe.com/reaction/1021063

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorideHCID 312—
反応物TetrahydrofuranHCID 8028—
反応物Ammonium ChlorideHCID 25517—
反応物1-(Phenylmethyl)-2,5-pyrrolidinedioneHCID 95241—
生成物1-Benzyl-5-biphenyl-4-ylmethyl-5-hydroxy-pyrrolidin-2-oneHCID 59318465—

反応条件

温度-78 °C

反応手順

9.5 g N-Benzylsuccinimide is added to 120 ml THF and the mixture is then cooled to −78° C. A solution of 4-methylbiphenylmagnesium chloride in THF (1.3 eq) is then added. The subsequent mixture is then stirred for 2 h at −78° C. The mixture is then warmed to 10° C. and 100 ml saturated ammonium chloride solution is added. The phases are separated and the aqueous phase is extracted with toluene. The combined organic phases are washed with water then brine and then concentrated in vacuo. The crude material is crystallized from toluene to give 1-Benzyl-5-biphenyl-4-ylmethyl-5-hydroxy-pyrrolidin-2-one. 1H NMR (DMSO): 1.72 (1H), 1.91 (1H), 2.27 (2H), 2.72 (1H), 2.97 (2H), 4.40 (1H), 4.55 (1H), 7.21-7.66 (14H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716495B2
出典データセットuspto-grants-2014_05
ORD IDord-54d4e0fc11c94b60b81a3174a2b36bbf
出典メモuspto-grants-2014_05