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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101488Generated: October 29, 2026

Benzene → Benzyl-{1-[1-(3,5-dichloro-benzyl)-1H-imidazol-2-yl]-ethyl}-amine

https://huagongshe.com/reaction/2101488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBenzylamineHCID 7504—
Reactant1-(3,5-dichloro-benzyl)-1H-imidazole-2-carbaldehydeHCID 57801490—
ProductBenzyl-{1-[1-(3,5-dichloro-benzyl)-1H-imidazol-2-yl]-ethyl}-amineHCID 1195196133%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1-(3,5-dichloro-benzyl)-1H-imidazole-2-carbaldehyde (see Example 2) (128 mg, 0.50 mmol), benzylamine (64 mg, 0.60 mmol), 3A molecular sieves (100 mg) and benzene (5 mL) was refluxed under N2 for 3 h. After cooling, the mixture was filtered and the filtrate concentrated in vacuo. The crude imine was dissolved in dry THF (3 mL) and the solution cooled to 0° C. before addition of MeMgBr (0.2 mL of a 3N solution in THF, 0.6 mmol). The resulting mixture was stirred at 0° C. for 1 h and then quenched with saturated NH4Cl (2 mL). After diluting with water (10 mL), the mixture was extracted with CH2Cl2 (2×40 mL). The combined CH2Cl2 extracts were dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (silica gel, 40:1 to 20:1 CH2Cl2/MeOH) to provide the title compound (60 mg, 33%) as a colorless oil: ESI MS m/z 360 [C19H19Cl2N2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572921B2
Source datasetuspto-grants-2009_08
ORD IDord-bf39bb13cd6849369056cdfc91e6f026
Source noteuspto-grants-2009_08