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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878417Generated: October 27, 2026

Sodium Iodide → tert-Butyl 4-(3-(1,1,1-trifluoro-2-methylpropan-2-ylcarbamoyl)benzyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1878417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-(chloromethyl)-N-(1,1,1-trifluoro-2-methylpropan-2-yl)benzamideHCID 66878349—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(3-(1,1,1-trifluoro-2-methylpropan-2-ylcarbamoyl)benzyl)piperazine-1-carboxylateHCID 8663513697.6%

Reaction Steps

3-(Chloromethyl)-N-(1,1,1-trifluoro-2-methylpropan-2-yl)benzamide (3.10 mmol, 868 mg), tert-butyl piperazine-1-carboxylate (3.10 mmol, 578 mg), sodium iodide (3.10 mmol, 465 mg) and triethylamine (3.10 mmol, 0.433 mL) were all combined in actetonitrile (28 ml) and heated to reflux for 2 hours. After this time the reaction mixture was allowed to cool and ethyl acetate and water were added. The organic layer was separated, dried and concentrated under vacuum to yield the title compound (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-890a1e933f444017af32c53d01b63d69
Source noteuspto-grants-2012_11