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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601553Generated: October 26, 2026

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

https://huagongshe.com/reaction/601553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant2-MethylallylamineHCID 76141—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
ProductN-Benzyl-2-methylprop-2-en-1-amineHCID 1378848492%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902356B2
Source datasetuspto-grants-2011_03
ORD IDord-bc213b058d0e477881d92474aec3da87
Source noteuspto-grants-2011_03