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HRID 1097728作成日:2026年10月27日

1,4-Dibromobutane → 3-(4-Bromobutyl)-1-(phenylmethyl)-2-pyrrolidinone

https://huagongshe.com/reaction/1097728

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DibromobutaneHCID 8056—
反応物1-Benzyl-3-pyrrolidoneHCID 79176—
反応物2-(Phenylmethyl)-2-azaspiro[4.4]nonan-1-oneHCID 15707438—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-Bromobutyl)-1-(phenylmethyl)-2-pyrrolidinoneHCID 59395857—

反応手順

To a solution of 1-(phenylmethyl)-2-pyrrolidinone (0.47 g, 2.7 mmol) in THF (10 ml) at −78° C. was added lithium hexamethyldisilylazine (2.8 ml, 2.7 mmol, 1M solution) over 5 min. After 15 min 1,4-dibromobutane (0.32 ml, 2.7 mmol) was added and the solution allowed to attain ambient temperature over 2 h then stirred for a further 18 h. The solution was separated between ethyl acetate and water and the organics isolated, dried and concentrated. Chromatography over silica (20 g SPE) eluting with cyclohexane then DCM and finally ether provided a clear oil which was a 1:1 mixture of the title compound and 2-(phenylmethyl)-2-azaspiro[4.4]nonan-1-one (0.17 g). This was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143264B2
出典データセットuspto-grants-2012_03
ORD IDord-d7f2e482a58640648abc361619115a0f
出典メモuspto-grants-2012_03