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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535004Generated: October 30, 2026

Water → HCID 66792770, compound

https://huagongshe.com/reaction/535004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant1-(2-Tert-butylphenyl)piperazine dihydrochlorideHCID 66751149—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66792770HCID 66792770—

Reaction Steps

A mixture of 1-(2-tert-butylphenyl)piperazine dihydrochloride obtained in Reference Example 1 (1.00 g, 3.42 mmol), 4-nitrobenzoyl chloride (0.761 g, 4.1 mmol) and triethylamine (1.67 mL, 12.0 mmol) in tetrahydrofuran (25 mL) was stirred at room temperature for overnight. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give a solid. A mixture of the obtained solid and 10% of palladium-carbon (100 mg) in tetrahydrofuran (30 mL) and methanol (100 mL) was stirred at room temperature under hydrogen atmosphere (5 atm). After being stirred for 3 h, the reaction mixture was filtrated and concentrated to purify the residue by NH-silica gel column chromatography (hexane/ethyl acetate 0:100) and the title compound was obtained as a solid (1.28 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-a5ae6296a1c04d2f8bf237da24b118e5
Source noteuspto-grants-2014_10