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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435832Generated: October 30, 2026

Methylamine → {4-[(Methylamino)methyl]phenyl}(phenyl)methanone

https://huagongshe.com/reaction/435832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(Bromomethyl)benzophenoneHCID 122951—
SolventBenzeneHCID 241—
Product{4-[(Methylamino)methyl]phenyl}(phenyl)methanoneHCID 15334722—

Reaction Steps

A solution of 12.0 g. (0.379 mole) anhydrous methyl amine in 150 ml. benzene is treated dropwise with 34.8 g. (0.127 mole) α-bromo-p-benzoyl toluene in 300 ml. benzene for about 30 minutes. The resulting mixture is stirred for 4 hours at room temperature and the solvent removed in vacuo. The resulting residue is dissolved in ether and washed with water. The ether layer is then extracted three times with 2N hydrochloric acid and the acidic solution made basic by the addition of potassium hydroxide and extracted with ether. The ether layer is washed with water, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue is then chromatographed on silica gel to yield 4-benzoyl N-methyl benzyl amine (identified by spectral analysis).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006248
Source datasetuspto-grants-1977_02
ORD IDord-1fcf0d4ec13041f48604d3a8cee7ba53
Source noteuspto-grants-1977_02