Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68615Generated: October 25, 2026

Methylamine → (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

https://huagongshe.com/reaction/68615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Bromo-4-((4-methoxybenzyl)oxy)benzaldehydeHCID 23010223—
SolventMethanolHCID 887—
Product(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamineHCID 6304514788%

Reaction Steps

To a solution of 2M methylamine in MeOH (30 mL) was added intermediate 32 (2.91 g, 9.1 mmol, 1 eq). After stirring this mixture at room temperature for 30 min, the solvent was removed and the residue was partitioned between saturated NaHCO3 and DCM (2×100 mL). The organic layer was dried (Na2SO4) and concentrated. The resultant residue was dissolved in MeOH (25 mL) and, after addition of sodium borohydride (1.0 g, 27.6 mmol, 3 eq), the mixture was stirred at room temperature for 1 h. Solvent was removed and the residue was partitioned between a Na2CO3 solution and CHCl3. The resultant organic layer was dried (Na2SO4) and concentrated in vacuo to give 2.7 g, (88%) of (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine (33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822467B2
Source datasetuspto-grants-2014_09
ORD IDord-2e2bdbd81f0c4e6ea906aa73e3b13f53
Source noteuspto-grants-2014_09