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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812021Generated: October 31, 2026

Potassium Carbonate → potassium (R)-((4-(tert-butoxycarbonyl)-2-methylpiperazin-1-yl)methyl)trifluoroborate

https://huagongshe.com/reaction/1812021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-1-Boc-3-methylpiperazineHCID 2756811—
ReactantPotassium (bromomethyl)trifluoroborateHCID 23690312—
SolventTetrahydrofuranHCID 8028—
Productpotassium (R)-((4-(tert-butoxycarbonyl)-2-methylpiperazin-1-yl)methyl)trifluoroborateHCID 7150191594.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of potassium (bromomethyl)trifluoroborate (1.20 g, 5.38 mmol) and (R)-4-N-Boc-2-methyl-piperazine (1.166 g, 5.65 mmol) in THF (7.00 mL) was heated at 80° C. under nitrogen for 24 h. After cooling, the mixture was concentrated, re-dissolved in acetone (125 mL) and treated with K2CO3 (1 eq). The suspension was stirred for 30 min and filtered through a short plug of Celite® (diatomaceous earth), washing with additional acetone and the combined organic phases were concentrated to give potassium (R)-((4-(tert-butoxycarbonyl)-2-methylpiperazin-1-yl)methyl)trifluoroborate as a pale yellow foam (1.627 g, 94%). 19F-NMR (377 MHz, d6-acetone) δ −141.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-edd7bf04dd164b8aa8592ad4b8882daf
Source noteuspto-grants-2013_01