Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339763Generated: October 30, 2026

Ethylenediamine → 3-(benzyloxy)-6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxyaniline

https://huagongshe.com/reaction/339763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantSulfurHCID 5362487—
Reactant2-Amino-4-(benzyloxy)-3-methoxybenzonitrileHCID 58219849—
Product3-(benzyloxy)-6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxyanilineHCID 705926886%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-amino-4-(benzyloxy)-3-methoxybenzonitrile (144 g, 566 mmol) and sulfur (55 g, 1.7 mol) in ethylenediamine (800 mL) was degassed for 30 minutes then heated to 100° C. After 16 h the reaction mixture was cooled to room temperature and then filtered. The filtrate was concentrated under reduced pressure, diluted with a saturated sodium bicarbonate solution and extracted with EtOAc. The organic layer was washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The resulting solids were recrystallized from EtOAc and hexanes to afford 3-(benzyloxy)-6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxyaniline (145 g, 86%): 1H NMR (DMSO-d6) δ: 7.27-7.48 (5H, m), 7.14 (1H, d), 6.92 (2H, m), 6.64 (1H, m), 6.32 (1H, d), 5.11 (2H, s), 3.67 (3H, s), 3.33 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895549B2
Source datasetuspto-grants-2014_11
ORD IDord-2830c86b09bc436e857003d7fbd58c89
Source noteuspto-grants-2014_11