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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496622Generated: October 30, 2026

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

https://huagongshe.com/reaction/496622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(bromoacetyl)piperazine-1-carboxylateHCID 1582915593%

Reaction Steps

To a stirring solution of bromoacetyl bromide (29.8 g, 148 mmol) in THF (250 mL) at 0° C. was added via an addition funnel a solution of Boc-piperazine (25 g, 134 mmol) and triethylamine (14.9 g, 148 mmol) in THF (75 mL). After 1 h, a few grams of ice were added and the mixture was diluted with ethyl acetate and cold water. The layers were separated and the organic phase was washed with 1 M aq. citric acid, brine, satd aq. NaHCO3 and again with brine. The organic phase was then dried with MgSO4, filtered, and concentrated in vacuo to give 38.2 g (93%) of an off-white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946467B2
Source datasetuspto-grants-2005_09
ORD IDord-b397f30741ae4f2b9f1f54f87be37dcd
Source noteuspto-grants-2005_09