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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694880Generated: October 31, 2026

Bromoacetyl bromide → tert-Butyl 4-(bromoacetyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1694880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(bromoacetyl)piperazine-1-carboxylateHCID 1582915541.2%

Reaction Steps

Bromo acetyl bromide (4.86 ml, 21.47 mmol, 1 eq) was added dropwise to a stirred ice cold mixture of the Piperazine-1-carboxylic acid tert butyl ester (4.0 g, 21.47 mmol, 1 eq) and diisopropyl ethyl amine (12.05 g, 92.5 mmol, 4.3 eq) in dichloromethane (108 ml). The resulting mixture was washed with water (2×50 mL) and saturated sodium chloride solution (100 mL), and dried over MgSO4. After filtration, the solvent was evaporated and the residue was purified with chromatography with (ethyl acetate/n-hexane 1/1) to give the product (2.72 g, 41%) as a orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158797B2
Source datasetuspto-grants-2012_04
ORD IDord-99fc77e2c8a9490c8491c265c0e2cd5b
Source noteuspto-grants-2012_04