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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730559Generated: October 26, 2026

Benzylamine → Benzyl-(3-benzyloxy-2-nitro-phenyl)-amine

https://huagongshe.com/reaction/730559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Benzyloxy)-3-fluoro-2-nitrobenzeneHCID 57834982—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl-(3-benzyloxy-2-nitro-phenyl)-amineHCID 2125474388%

Reaction Conditions

Temperature110 °C

Reaction Steps

Potassium carbonate (5.71 g., 41.4 mmol) was added to a solution of 1-benzyloxy-3-fluoro-2-nitro-benzene (6.818 g, 27.6 mmol) and benzylamine (3.32 mL, 30.34 mmol) in tetrahydrofuran, and the resulting suspension was heated to 110° C. for 2 hours. After cooling to room temperature, the mixture was poured onto 1 L of ice water and extracted twice with 150 mL ethyl acetate and twice with 75 mL dichloromethane. The combined organic fractions were dried over sodium sulfate and concentrated in vacuo in the presence of 25 g. silica gel. The preloaded silica gel was submitted to flash chromatography (8% to 35% ethyl acetate in hexanes) to give 8.118 g (24.28 mmol, 88%) of benzyl-(3-benzyloxy-2-nitro-phenyl)-amine as an orange solid. MS: 335 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582760B2
Source datasetuspto-grants-2009_09
ORD IDord-922b7aaf4a9844d9920e6fbfe9ca6c46
Source noteuspto-grants-2009_09