戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 469289作成日:2026年10月25日

Acetic Acid → (1-Benzylpiperidin-4-yl)-[2-(5-methoxy-2-nitrophenyl)-ethyl]-amine

https://huagongshe.com/reaction/469289

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Potassium CarbonateHCID 11430—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-Benzyl-2-piperidoneHCID 5170076—
反応物2-(5-Methoxy-2-nitrophenyl)ethan-1-amineHCID 18621975—
溶媒DichloromethaneHCID 6344—
生成物(1-Benzylpiperidin-4-yl)-[2-(5-methoxy-2-nitrophenyl)-ethyl]-amineHCID 21109931100%

反応条件

温度0 °C

反応手順

Under a nitrogen atmosphere a mixture of 9.98 g (50.9 mmol) 2-(5-methoxy-2-nitrophenyl)-ethylamine, 9.80 mL (54.9 mmol) N-benzylpiperidone and 6.30 mL (114 mmol) acetic acid in 270 mL DCM was cooled to 0° C. in an ice bath. At this temperature 14.2 g (67.0 mmol) sodium triacetoxyborohydride were added batchwise within 20 min. The reaction mixture was stirred for a further 4 h at 0° C. and left to warm up to RT overnight. Then the mixture was combined with 400 mL of a 15% (w/v) aqueous potassium carbonate solution and stirred for 1 h at RT. The organic phase was separated off, dried and concentrated by rotary evaporation. 18.8 g of the desired product were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629137B2
出典データセットuspto-grants-2014_01
ORD IDord-3e1c2f221c9e4506885fd66d5bd83c5b
出典メモuspto-grants-2014_01