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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37834Generated: October 25, 2026

1-Chloro-4-nitrobenzene → 1-(4-Nitrophenyl)-1,4-diazepane

https://huagongshe.com/reaction/37834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-nitrobenzeneHCID 7474—
ReactantHexahydro-1,4-diazepineHCID 68163—
Solvent1-ButanolHCID 263—
Product1-(4-Nitrophenyl)-1,4-diazepaneHCID 505595042%

Reaction Steps

A solution of homopiperazine (11.4 g, 114 mmol) in 1-butanol (40 mL) was added to a refluxing solution of 1-chloro-4-nitrobenzene (6.0 g, 38 mmol) in 1-butanol (40 mL) over 15 minutes. The mixture was maintained at reflux for 24 hours then cooled to room temperature and extracted with 2N hydrochloric acid. The aqueous layer was basified with potassium carbonate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated to afford 1-(4-nitro-phenyl)-[1,4]diazepane (3.5 g, 42%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524705B2
Source datasetuspto-grants-2013_09
ORD IDord-4c60e14d135f433dad7b2bd9ef175647
Source noteuspto-grants-2013_09