Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539727Generated: October 31, 2026

1,2-Dichloroethane → HCID 57597100, compound

https://huagongshe.com/reaction/539727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant3-Nitrophenylacetic acidHCID 15876—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventEthyl AcetateHCID 8857—
ProductHCID 57597100HCID 57597100—

Reaction Steps

An oven-dried, round-bottom flask was charged with tert-butyl piperazine-1-carboxylate (1.1 eq), 3-nitrophenylacetic acid (7A, 1.0 eq), EDC (1.2 eq), and HOBT (1.2 eq). The flask was flushed with nitrogen, and N,N-dimethylformamide (about 0.5 M 7A in DMF) and triethylamine (2.0 eq) were added by syringe. The resulting reaction mixture was stirred overnight at room temperature. The reaction mixture was then diluted with EtOAc, and washed 4 times with H2O, twice with 1 N aq. KIHSO4, once with saturated NaHCO3, and once with brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. Tert-butyl 4-(2-(3-nitrophenyl)acetyl)piperazine-1-carboxylate (7B) was isolated as a solid (80%) and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871769B2
Source datasetuspto-grants-2014_10
ORD IDord-998521ecc8c346ad82a0160df48a0a0d
Source noteuspto-grants-2014_10