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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Benzyloxy)-3-fluoro-2-nitrobenzene | HCID 57834982 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl-(3-benzyloxy-2-nitro-phenyl)-amine | HCID 21254743 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07582760B2 |
|---|
| Source dataset | uspto-grants-2009_09 |
|---|
| ORD ID | ord-922b7aaf4a9844d9920e6fbfe9ca6c46 |
|---|
| Source note | uspto-grants-2009_09 |
|---|