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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601553생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/601553

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물2-MethylallylamineHCID 76141—
반응물Sodium borohydrideHCID 4311764—
용매TetrahydrofuranHCID 8028—
생성물N-Benzyl-2-methylprop-2-en-1-amineHCID 1378848492%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902356B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-bc213b058d0e477881d92474aec3da87
출처 메모uspto-grants-2011_03