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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38247Generated: October 25, 2026

Triethylamine → 1-[4-(2-Chloro-4-nitrophenyl)piperazin-1-yl]-2-methylpropan-1-one

https://huagongshe.com/reaction/38247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
Reactant1-(2-Chloro-4-nitrophenyl)piperazineHCID 2771331—
SolventDichloromethaneHCID 6344—
Product1-[4-(2-Chloro-4-nitrophenyl)piperazin-1-yl]-2-methylpropan-1-oneHCID 2886337100%

Reaction Steps

According to Scheme 4 Step 1: Isobutyryl chloride (1.24 mmol, 0.13 mL) and Et3N (2.48 mmol, 0.35 mL) were added to a solution of 1-(2-chloro-4-nitrophenyl)piperazine (0.83 mmol, 200 mg) in DCM (5 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure to afford 1-(4-(2-chloro-4-nitrophenyl)piperazin-1-yl)-2-methylpropan-1-one (0.83 mmol, 261 mg, 100%). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524726B2
Source datasetuspto-grants-2013_09
ORD IDord-20b164a09da742bea74ca466d122cbe8
Source noteuspto-grants-2013_09