Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031967Generated: October 26, 2026

N-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamine → N-methyl-N-(5-aminobenzoxazol-2-ylmethyl)-4-aminophenethylamine

https://huagongshe.com/reaction/1031967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamineHCID 19813428—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductN-methyl-N-(5-aminobenzoxazol-2-ylmethyl)-4-aminophenethylamineHCID 19813431—

Reaction Steps

N-Methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamine (0.78 g,2.2 mmole) in ethanol (50 ml) containing Raney nickel (0.1 g) was stirred under a hydrogen atmosphere (50 psi=344.7 kPa) for 18 hours, by which time thin layer chromatographic analysis showed that all the starting material had been consumed [silica chromatography plates using methylene chloride/methanol (19:1) as the solvent]. The reaction mixture was then filtered and evaporated to give an oil which was azeotroped with toluene and triturated with ether. The decanted ether was evaporated to give the title compound as an oil, which was used directly without further purification, yield 0.45 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956382
Source datasetuspto-grants-1990_09
ORD IDord-b2201bf1b6d5481e82aaea51315d3fec
Source noteuspto-grants-1990_09