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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535024Generated: October 31, 2026

Water → 1-[(4-Bromophenyl)carbonyl]-4-(2-tert-butylphenyl)piperazine

https://huagongshe.com/reaction/535024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Bromobenzoyl chlorideHCID 68515—
Reactant1-(2-Tert-butylphenyl)piperazine dihydrochlorideHCID 66751149—
SolventTetrahydrofuranHCID 8028—
Product1-[(4-Bromophenyl)carbonyl]-4-(2-tert-butylphenyl)piperazineHCID 66750884—

Reaction Steps

A mixture of 1-(2-tert-butylphenyl)piperazine dihydrochloride obtained in Reference Example 1 (10.0 g, 34.3 mmol), 4-bromobenzoyl chloride (8.2 g, 37.4 mmol) and triethylamine (16.7 mL, 120.0 mmol) in tetrahydrofuran (200 mL) was stirred at room temperature for 16 h. 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 purify the residue by NH-silica gel column chromatography (hexane/ethyl acetate 50:50 to 0:100). Solvent was removed to obtain a solid (14.2 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-152180fdf31b407996c90b122f6e2224
Source noteuspto-grants-2014_10