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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713076Generated: October 27, 2026

Sodium Bicarbonate → 1-(Chloroacetyl)-4-cyclobutylpiperazine

https://huagongshe.com/reaction/1713076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-CyclobutylpiperazineHCID 4738602—
ReactantChloroacetyl bromideHCID 12610899—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(Chloroacetyl)-4-cyclobutylpiperazineHCID 57420562—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of sodium bicarbonate (15 mmol) in water (5 mL) and DCM (30 mL) at 0° C. is added chloroacetyl bromide (12 mmol), followed by immediate addition of 1-cyclobutylpiperazine (10 mmol). The mixture is stirred at 0° C. for an additional 40 min. To the mixture is added aqueous sodium bicarbonate (15 mL) and DCM (30 mL). The layers are separated and the organic layer is dried (MgSO4) and solvent is removed in vacuo to give 2-chloro-1-(4-cyclobutyl-piperazin-1-yl)-ethanone, which is used in the next step without further purification. 1H NMR (300 MHz, CDCl3) δ 4.07 (2H, s), 3.64 (2H, t), 3.52 (2H, t), 2.74 (1H, m), 2.36 (2H, t), 2.31 (2H, t), 1.72-2.08 (6H, m); MS (+VE) m/z 217.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795262B2
Source datasetuspto-grants-2010_09
ORD IDord-8e4abdf4a7e44e8998d6a9f474db4b00
Source noteuspto-grants-2010_09