Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337663Generated: October 29, 2026

Sulfuric acid magnesium salt (1:1) → N-{3-Bromo-5-[(1E)-3-methoxy-1-propen-1-yl]-4-methylbenzyl}cyclopropanamine

https://huagongshe.com/reaction/337663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantCyclopropylamineHCID 69828—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Bromo-5-[(1E)-3-methoxy-1-propen-1-yl]-4-methylbenzaldehydeHCID 87254203—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductN-{3-Bromo-5-[(1E)-3-methoxy-1-propen-1-yl]-4-methylbenzyl}cyclopropanamineHCID 66895831—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromo-5-[(1E)-3-methoxy-1-propen-1-yl]-4-methylbenzaldehyde (1 eq.) from the previous step and cyclopropylamine (2 eq.) were combined in CH2Cl2 (0.1 M). To this was then added MgSO4 (1 eq.) and the resulting suspension was stirred at RT for 20 h. The insolubles were then removed via filtration through a pad of celite and the filtrate was concentrated in vacuo. The crude imine thus obtained was then re-taken up in MeOH (0.1 M). To this solution was added sodium borohydride (1.5 eq.) portionwise and the resulting mixture was stirred at 0° C. for 30 min, then at RT for 2 h. The reaction was quenched by stirring with 2 N aq. HCl for 25 min, basified with 1 N aq. NaOH and concentrated in vacuo. The residue was extracted with ether from water, dried over Na2SO4, filtered and the filtrate concentrated in vacuo to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-b05b6803a6534bcabdbecdefa52eb13a
Source noteuspto-grants-2014_11