HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402555Generated: November 1, 2026
3-benzyloxy-2-nitro-N-methylaniline → 3-benzyloxy-N1-methylbenzene-1,2-diamine hydrochloride
https://huagongshe.com/reaction/2402555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-benzyloxy-2-nitro-N-methylaniline | HCID 10729890 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Catalyst | HCID 178503042 | HCID 178503042 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-benzyloxy-N1-methylbenzene-1,2-diamine hydrochloride | HCID 67954038 | 85% |
Reaction Steps
0.80 g of 5% platinum carbon (dry) was added to a toluene (80 mL) suspension of 3-benzyloxy-N-methyl-2-nitroaniline (7.19 g, 27.8 mmol), and catalytic hydrogenation reaction was performed under ordinary pressure. The reaction solution was filtered to remove a catalyst, and the catalyst was washed with toluene (10 mL). The washing liquid was added to the precedent filtrate. A 1N hydrochloric acid ethanol solution (28 mL, 28.0 mmol) was added to the mixture under ice cooling, and the mixture was stirred under the same temperature for 30 minutes. The solvent was distilled off under reduced pressure at 20° C. or less. Precipitated crystals were collected by filtration, washed with toluene (15 mL), and dried at 40° C., thereby obtaining 6.30 g of an orange, crystal target compound (yield: 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08796447B2 |
|---|
| Source dataset | uspto-grants-2014_08 |
|---|
| ORD ID | ord-e815e0b29aa44e35b34446f782c51bbc |
|---|
| Source note | uspto-grants-2014_08 |
|---|