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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421834Generated: October 31, 2026

Chloroform → tert-Butyl 4-(bromoacetyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/421834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(bromoacetyl)piperazine-1-carboxylateHCID 15829155—

Reaction Steps

With cooling with ice, bromoacetyl bromide (680 μL) was added to a chloroform (10 ml) solution of 1-tert-butyloxycarbonylpiperazine (1 g) and triethylamine (2.2 mL). At that temperature, this was stirred for 0.5 hours, and then at room temperature for further 0.5 hours. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline water, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=7/3) to obtain 340 mg of the entitled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101618B2
Source datasetuspto-grants-2012_01
ORD IDord-416098bc7ea845c8b9890c1bae4291e0
Source noteuspto-grants-2012_01