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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670743Generated: October 27, 2026

Ethylene Glycol → 1-Boc-4-(2-thienyl)piperazine

https://huagongshe.com/reaction/1670743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant2-IodothiopheneHCID 18921—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product1-Boc-4-(2-thienyl)piperazineHCID 6734390077%

Reaction Steps

A mixture of 2-iodothiophene (Aldrich Co., 1.0 g), 1-(tert-butoxycarbonyl)piperazine (Aldrich Co. (hereafter the same), 1.06 g), copper(I) iodide (45 mg), ethylene glycol (530 μl), potassium phosphate (2.02 g) and 2-propanol (5 ml) was heated under reflux for 20 hr. Ethyl acetate was added, and the mixture was filtered through a Celite (trademark) filter. The filtrate was washed 3 times with 28% aqueous ammonia, and then washed with saturated brine. The solvent was evaporated under reduced pressure to give a brown solid. The solid was purified by silica gel column chromatography (elution solvent: ethyl acetate-hexane (7:3)) to give 4-(2-thienyl)piperazine-1-carboxylic acid tert-butyl ester (984 mg, yield 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994196B2
Source datasetuspto-grants-2011_08
ORD IDord-ffc748b1030f4f6abf2f239762f169db
Source noteuspto-grants-2011_08