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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356218Generated: November 2, 2026

Triethylamine → HCID 58724166, compound

https://huagongshe.com/reaction/2356218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 62389644HCID 62389644—
SolventDichloromethaneHCID 6344—
ProductHCID 58724166HCID 58724166—

Reaction Steps

Ethyl 1-(piperazin-1-yl)cyclobutanecarboxylate (0.71 mmol) was dissolved in CH2Cl2 (5 ml). Triethylamine (0.30 ml, 2.1 mmol), followed by 2-chlorobenzenesulfonyl chloride (0.11 ml, 0.79 mmol), was added at room temperature. The orange-colored solution was stirred at room temperature for 6 h before saturated NaHCO3 solution was added. The mixture was extracted twice with EtOAc. Combined organic layers were washed once with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (SiO2, gradient 5-10% Et2O/CH2Cl2) to give ethyl 1-(4-(2-chlorophenylsulfonyl)piperazin-1-yl)cyclobutanecarboxylate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759339B2
Source datasetuspto-grants-2010_07
ORD IDord-d31bd8a72ab645348bfec9dd24aab8d9
Source noteuspto-grants-2010_07