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HRID 1694407作成日:2026年10月27日

Pyrrolidine → 1-(3,5-Difluorobenzyl)pyrrolidine

https://huagongshe.com/reaction/1694407

反応式

関与物質

役割名称HCID仕込み量
反応物PyrrolidineHCID 31268—
反応物Sodium BicarbonateHCID 516892—
反応物3,5-DifluorobenzaldehydeHCID 588160—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(3,5-Difluorobenzyl)pyrrolidineHCID 6727925274%

反応手順

3,5-Difluorobenzaldehyde (2.0 mL, 18.24 mmol), pyrrolidine (1.8 mL, 21.56 mmol), and sodium triacetoxyborohydride (5.8 g, 27.4 mmol) were stirred in THF (50 mL) for 16 h at room temperature. Saturated aqueous NaHCO3 (30 mL) was added and after stirring for 30 min, EtOAc (50 mL) was added. The organic phase was separated and washed with brine, dried over MgSO4 and concentrated to afford 2.65 g (74%) of 1-(3,5-difluorobenzyl)pyrrolidine as a slightly cloudy oil: 1H NMR (CDCl3) δ 6.88-6.83 (m, 1H), 6.68-6.63 (m, 2H), 3.59 (s, 2H), 2.53-2.48 (m, 4H), 1.80-1.77 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08158673B2
出典データセットuspto-grants-2012_04
ORD IDord-2090fbbe074e4ccebf96bc4aa6be1629
出典メモuspto-grants-2012_04