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HRID 601553作成日:2026年10月26日

Benzaldehyde → N-Benzyl-2-methylprop-2-en-1-amine

https://huagongshe.com/reaction/601553

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物2-MethylallylamineHCID 76141—
反応物Sodium borohydrideHCID 4311764—
溶媒TetrahydrofuranHCID 8028—
生成物N-Benzyl-2-methylprop-2-en-1-amineHCID 1378848492%

反応手順

Add benzaldehyde (14.5 mL, 143 mmol) to a mixture of methallylamine (9.73 g, 137 mmol) and MgSO4 (15.0 g, 125 mmol) in THF (180 mL). Stir for 22 h, filter the mixture, and concentrate the filtrate. Dissolve the residue in EtOH (200 mL) and treat with NaBH4 (5.00 g, 132 mmol) in 3 portions. After 19 h, remove the solvent by rotary evaporation. Treat the residue with 1 M HCl (200 mL) then 5 M HCl (20 mL). Wash the solution with tert-butyl methyl ether (250 mL) and then treat with 5 M NaOH (50 mL) to make basic. Extract the mixture with CH2Cl2 (200 mL followed by 100 mL). Dry, filter and concentrate the organic solution to give the title compound (20.3 g, 92%) as a colorless liquid. 1H NMR (400 MHz, DMSO-d6): δ 7.2-7.4 (5H, m), 4.84 (1H, s), 4.79 (1H, s), 3.63 (2H, s), 3.03 (2H, s), 1.69 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902356B2
出典データセットuspto-grants-2011_03
ORD IDord-bc213b058d0e477881d92474aec3da87
出典メモuspto-grants-2011_03