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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284674Generated: October 31, 2026

3-Nitroaniline → HCID 90052093, compound

https://huagongshe.com/reaction/2284674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitroanilineHCID 7423—
ReactantSodium BicarbonateHCID 516892—
ReactantN-Boc-hexahydro-1H-azepin-4-oneHCID 1512679—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 90052093HCID 9005209371.1%

Reaction Steps

To a solution of N-Boc-hexahydro-1H-azepin-4-one (141 mg) and 3-nitroaniline (91 mg) in methylene chloride (3 mL), sodium triacetoxyborohydride (210 mg) and acetic acid (38 μL) were added at room temperature, and the mixture was stirred at the same temperature for 10 hours. To the reaction mixture, ethyl acetate and saturated aqueous sodium hydrogencarbonate were added. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 100 to 30% hexane in ethyl acetate) to obtain tert-butyl 4-((3-nitrophenyl)amino)azepane-1-carboxylate (C25, 157 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-d3a79e311bfc4b8bbae8b6c9c55a74b9
Source noteuspto-grants-2015_09