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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534898Generated: October 30, 2026

Tetrahydrofuran → Methyl 4-{[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}benzoate

https://huagongshe.com/reaction/534898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-(chlorocarbonyl)benzoateHCID 81850—
Reactant1-(2-Tert-butylphenyl)piperazine dihydrochlorideHCID 66751149—
SolventWaterHCID 962—
ProductMethyl 4-{[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}benzoateHCID 6675132396%

Reaction Steps

A mixture of 1-(2-tert-butylphenyl)piperazine dihydrochloride obtained in Reference Example 1 (0.5 g), methyl 4-(chlorocarbonyl)benzoate (397 mg), triethylamine (0.836 mL), and tetrahydrofuran (10 mL) was stirred at room temperature for over-night. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by flash column chromatography (NH-silica gel, 90:10-50:50 hexane/ethyl acetate) to provide the title compound (628 mg, 96%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-b1e00b7b61354c4aab2a328494c72752
Source noteuspto-grants-2014_10