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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401338Generated: October 31, 2026

2-Methoxyethylamine → N-((6-Bromopyridin-2-yl)methyl)-2-methoxyethanamine

https://huagongshe.com/reaction/1401338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductN-((6-Bromopyridin-2-yl)methyl)-2-methoxyethanamineHCID 5796727896%

Reaction Steps

A mixture of 6-bromo-2-pyridinecarboxaldehyde (54) (20 g, 108 mmol) and 2-methoxy ethanamine (10.3 mL, 8.88 g, 118 mmol) in DCM (1.3 L) was stirred at room temperature for 10 min. It was then treated with NaBH(OAc)3 (25 g, 118 mmol) and stirred at room temperature overnight. The reaction mixture was quenched with water (400 mL) and acidified to pH=4 with 1M HCl (˜140 mL). The two phases were separated and the organic layer was extracted with 0.25M HCl (2×500 mL). The aqueous layers were combined, basified to pH=9 with 4N NaOH, extracted with DCM (1×500 mL), dried over Na2SO4, filtered and concentrated yielding 25.2 g of 55 (96%). MS (m/z): 245.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907091B2
Source datasetuspto-grants-2014_12
ORD IDord-d8f0c27cebbf4833ab8c95d831fa6ac8
Source noteuspto-grants-2014_12