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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056923Generated: October 25, 2026

Benzaldehyde → Benzylidene-(3-bromo-1-propylamine)

https://huagongshe.com/reaction/1056923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTriethylamineHCID 8471—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant3-BromopropylamineHCID 78702—
SolventChloroformHCID 6212—
ProductBenzylidene-(3-bromo-1-propylamine)HCID 11053338100%

Reaction Steps

The hydrobromide salt of 3-bromopropylamine (5.364 g, 24.50 mmol) was treated with triethylamine (4 mL) in CHCl3 (100 mL) and allowed to stir at room temperature for 5 min. Benzaldehyde (2.000 g, 18.85 mmol) and magnesium sulfate (6.000 g) were added and the reaction mixture was allowed to stir at room temperature for 16 h. The reaction mixture was filtered and the filter pad was washed with CHCl3 (50 mL). The filtrate was washed with water (3×50 mL), sat NaCl (50 mL), dried over sodium sulfate, and concentrated to provide a yellow oil (4.262 g, 100%). IR (film) 1645, 754, and 693 cm−1; 1H NMR (CDCl3) δ 8.34 (s, 1H), 7.76 (m, 2H), 7.44 (m, 3H), 3.78 (dt, J=6.3 Hz and 1.3 Hz, 2H), 3.52 (t, J=6.5 Hz, 2H), 2.31 (pent, J=6.4 Hz, 2H); ESIMS m/z (rel intensity) 226/228 (MH+, 100/91). Anal. (C10H12BrN) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399660B2
Source datasetuspto-grants-2016_07
ORD IDord-16deeed8a8bf44db90a43b8645e27a76
Source noteuspto-grants-2016_07