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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119358Generated: October 26, 2026

Acetyl chloride → 1-[(4-Chlorophenyl)methyl]-1,4-diazepane

https://huagongshe.com/reaction/2119358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantHexahydro-1,4-diazepineHCID 68163—
SolventEthanolHCID 702—
Product1-[(4-Chlorophenyl)methyl]-1,4-diazepaneHCID 1563437754.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

Acetyl chloride (11.7 mL, 0.165 mol) was added to anhydrous EtOH (500 mL) and the mixture was stirred for 30 min at 25° C. Homopiperazine (15.0 g, 0.150 mol) was added and the mixture was heated to reflux for 4 h. 4-Chlorobenzyl chloride (13.96 g, 0.087 mol) was added and the reaction mixture was heated to reflux for 16 h before concentrating. The residue was dissolved in EtOAc (500 mL) and washed with 1N aqueous KOH (50 mL). The aqueous layer was extracted with EtOAc (200 mL). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. Chromatography (double separation. SiO2, 20×7 cm, 1PrOH—H2O—NH4OH, 80:12:6 to 70:20:10 gradient elution) afforded the desired product (10.6 g, 53.4%) and the dialkylated homopiperazine (2.36 g, 16.5%). GC/MS m/e 224 (M+, C12H17N2Cl).10% CH3OH—CH2Cl2); RPLC tR=5.96 min (>85%), 220 nm (Mm (Method B): ESI/MS m/e 498.3 (MH++H, C31H35N3O3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686353B1
Source datasetuspto-grants-2004_02
ORD IDord-2cad4e417b304170a49e5ee79dde87c0
Source noteuspto-grants-2004_02