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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977489Generated: October 31, 2026

Methylamine → 2-Bromo-N-methylbenzylamine

https://huagongshe.com/reaction/1977489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-N-methylbenzylamineHCID 52236058%

Reaction Steps

29.4 g of o-Bromobenzaldehyde and 81 ml of aqueous, 40% methylamine solution are combined with 238 ml of THF and at RT 19 g of NaBH4 are added in batches within 25 minutes. The mixture is left to stand overnight at RT, concentrated using a rotary evaporator, and the residue is stirred into ice water. The aqueous phase is extracted twice with ether and the combined ether phases are evaporated down under reduced pressure. After chromatography on silica gel with ethyl acetate or ethyl acetate/methanol (4:1) as eluant, 18.5 g of N-methyl-2-bromobenzylamine (a) are obtained in the form of a yellowish liquid. Yield: 58%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232468B1
Source datasetuspto-grants-2001_05
ORD IDord-91ca148930ed4d8fa0b64a201b95cf33
Source noteuspto-grants-2001_05