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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878323Generated: November 2, 2026

4-Nitrobenzoyl chloride → HCID 66878228, compound

https://huagongshe.com/reaction/1878323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66878161HCID 66878161—
SolventDichloromethaneHCID 6344—
ProductHCID 66878228HCID 6687822894.9%

Reaction Steps

N-tert-Butyl-3-(piperazin-1-ylmethyl)benzamide dihydrochloride (0.50 g, 1.44 mmol) was suspended in stirred dichloromethane (20 mL) at 0° C. (ice-bath) under an argon atmosphere. N-ethyl-N-isopropylpropan-2-amine (1.0 mL, 5.75 mmol) was added slowly. After 10 minutes stirring, the resulting solution was treated with a suspension of 4-nitrobenzoyl chloride (0.267 g, 1.44 mmol) In dichloromethane (10 ml). The ice-bath was removed and stirring continued for 1 hour. The solution was diluted with dichloromethane (70 mL) and washed with water (×4). The organic phase was dried on magnesium sulfate, filtered and concentrated under vacuum to give the title compound (0.58 g) as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-dcc8ad27f44b450a80329b173a93e552
Source noteuspto-grants-2012_11