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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377619Generated: November 1, 2026

Benzylamine → HCID 57431197, compound

https://huagongshe.com/reaction/2377619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant4-Bromo-2,3-dimethylanisoleHCID 2752599—
ReactantHCID 86610194HCID 86610194—
SolventAcetonitrileHCID 6342—
ProductHCID 57431197HCID 5743119755%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 1-bromo-2,3-bis(bromomethyl)-4-methoxybenzene (prepared as described in J. Org. Chem. 1992, 57, 6374, from commercially available 1-bromo-4-methoxy-2,3-dimethylbenzene) in CH3CN (0.1 M) were added 2.5 eq of KHCO3 and the mixture heated at 60° C. Then 1 eq. of benzylamine in CH3CN (0.9 M) was added within 15 minutes and the mixture was heated to reflux for 2 h. The reaction mixture was allowed to cool, filtered over celite and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel (5% EtOAc in petroleum ether, then 10%) to afford the title compound (55%). 1H NMR (300 MHz, CDCl3, ppm) δ 3.77 (s, 3H), 3.92 (s, 2H), 3.98 (s, 2H), 4.01 (s, 2H), 6.60 (d, J 8.6, 1H), and 7.22-7.46 (m, 6H). MS (ES+) m/z 318, 320 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470664B2
Source datasetuspto-grants-2008_12
ORD IDord-21c0bb6665fb405f80573a79590679ec
Source noteuspto-grants-2008_12