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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499002Generated: October 26, 2026

Methylamine → [5-Bromo-2-(3,4-dichloro-phenoxy)-benzyl]-methyl-amine

https://huagongshe.com/reaction/499002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Bromo-2-(3,4-dichlorophenoxy)benzaldehydeHCID 12017030—
SolventMethanolHCID 887—
Product[5-Bromo-2-(3,4-dichloro-phenoxy)-benzyl]-methyl-amineHCID 994700997%

Reaction Steps

To a mixture of 5-bromo-2-(3,4-dichloro-phenoxy)-benzaldehyde (4.74 g, 13.8 mmol) in MeOH (250 mL) was added MeNH2 (40% aq.; 20 mL, 260 mmol), and the resulting mixture was stirred at rt until homogeneous. The mixture was cooled to 0° C. and treated with NaBH4 (1.05 g, 27.8 mmol) portionwise. After 24 h, the mixture was concentrated and the residue was diluted with 1 N NaOH and extracted with DCM. The combined organic layers were dried (Na2SO4) and concentrated. The crude product was purified by FCC to provide the desired product (4.80 g, 97%). MS (ESI): mass calcd. for C14H12BrCl2NO, 358.95; m/z found, 360.1 [M+H]+. 1H NMR (CDCl3): 7.61 (d, J=2.5, 1H), 7.40-7.37 (m, 2H), 7.03 (d, J=2.8, 1H), 6.82-6.79 (m, 2H), 3.72 (s, 2H), 2.44 (s, 3H), 1.30-1.21 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767666B2
Source datasetuspto-grants-2010_08
ORD IDord-3ae549d54a8b415bbc522d5b18171081
Source noteuspto-grants-2010_08