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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739749Generated: October 29, 2026

Acetyl chloride → Tert-butyl 4-acetylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1739749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-acetylpiperazine-1-carboxylateHCID 227070233.6%

Reaction Steps

To a solution of N-t-butoxycarbonylpiperazine (7 g, 1 mol. equiv.) in dichloromethane (140 ml) at 0° C. under nitrogen was added triethylamine (6.29 ml, 1.2 mol. equiv.). The reaction mixture was vigorously stirred and acetyl chloride (3.21 ml, 1.2 mol. equiv.) was added, dropwise. The mixture was stirred for twenty four hours. The reaction mixture was washed with saturated aqueous sodium bicarbonate solution (30 ml), and the organic layer dried using magnesium sulphate. The organic solvent was removed under reduced pressure and the residue purified by flash column chromatography on silica gel eluting with methanol:ethyl acetate (1:19, by volume) to give the title compound (8.19 g). TLC Rf=0.33 (silica, methanol:ethyl acetate, 1:19, by volume). LRMS m/z=229(m+1)+. Found: C, 57.83; H, 8.83; N, 12.27. C11H20N2O3 requires C, 57.87; H, 8.92; N, 12.14%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968923
Source datasetuspto-grants-1999_10
ORD IDord-d1bd4a63687440a1b3be5789c3160196
Source noteuspto-grants-1999_10