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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358387Generated: November 1, 2026

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

https://huagongshe.com/reaction/1358387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant5-Bromo-2-(3,4-dichlorophenoxy)benzaldehydeHCID 12017030—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
Product[5-Bromo-2-(3,4-dichloro-phenoxy)-benzyl]-methyl-amineHCID 9947009—

Reaction Steps

Under N2, a solution of methylamine (2.9 mL, 5.8 mmol, 2.0 M solution in CH3OH) in 20 mL of ethanol was treated with titanium (IV) isopropoxide (1.7 mL, 5.8 mmol) at room temperature. After 5 min., a suspension of 5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde (1.0 g, 2.9 mmol, the title compound of Preparation 1) in 20 mL of ethanol was added and stirred for 16 hr at room temperature. Sodium borohydride (0.165 g, 4.4 mmol) was then added and stirring was continued for an additional 24 hr, at which time the reaction was quenched by the addition of 5 mL of 6 N HCl and 5 mL of water, stirred for 30 min and made basic by the addition of saturated aqueous Na2CO3. The resulting mixture was extracted with EtOAc, and the organic extracts were clarified by filtration throught diatomaceous earth (d.e.), washed with saturated NaCl, dried over Na2CO3 and concentrated in vacuo to a clear oil, 0.987 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596741B2
Source datasetuspto-grants-2003_07
ORD IDord-303c1a0481e64d809ce019549aa0221e
Source noteuspto-grants-2003_07