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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784658Generated: October 30, 2026

Acetic Acid → tert-Butyl 2-(4-chlorophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1784658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67117397HCID 67117397—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl 2-(4-chlorophenyl)piperazine-1-carboxylateHCID 4455859969.5%

Reaction Steps

Solution of 4-(tert-butoxycarbonyl)-3-(4-chlorophenyl)-piperazin-2-one (500 mg, 1.6 mmol) and acetic acid (929 μl, 16 mmol) were added to a refluxed solution of sodium borohydride (608 mg, 16 mmol) in 1,4-dioxane (5 ml) and reflux was continued. The reaction was quenched by water and extracted with dichloromethane and washed with brine and dried. After removal of the solvent, residue was purified by silica gel column chromatography to give 4-(tert-butoxycarbonyl)-3-(4-chlorophenyl)piperazine (330 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504411B2
Source datasetuspto-grants-2009_03
ORD IDord-f3289adec1bb49b0b7ded17da9899ca1
Source noteuspto-grants-2009_03