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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429629Generated: October 25, 2026

Sodium Chloride → t-Butyl 5-methylpyrazine-2-carboxylate

https://huagongshe.com/reaction/1429629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantEthyl AcetateHCID 8857—
Reactant5-Methyl-2-pyrazinecarboxylic acidHCID 122831—
ReactantTert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
SolventTetrahydrofuranHCID 8028—
Productt-Butyl 5-methylpyrazine-2-carboxylateHCID 5747568399.6%

Reaction Steps

A boron trifluoride-diethyl ether complex (91.7 μL) was added dropwise to a suspension of 2-methylpyrazine-5-carboxylic acid (1 g) and tert-butyl 2,2,2-trichloroacetimidate (4.75 g) in THF (20 mL) under ice-cooling. The reaction solution was warmed to RT, followed by stirring for 2 h. A saturated NaCl solution and EtOAc were added to the reaction solution, and the organic layer was separated. The organic layer was dried over anhydrous MgSO4, and the insoluble matter was separated by filtration. The filtrate was concentrated and purified by silica gel column chromatography to obtain the title compound (1.4 g). 1H-NMR (CDCl3) δ (ppm): 1.65 (s, 9H), 2.65 (s, 3H), 8.57 (d, J=1.2 Hz, 1H), 9.10 (d, J=1.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940734B2
Source datasetuspto-grants-2015_01
ORD IDord-b063ab05f1214bfea7f83c5284f03e51
Source noteuspto-grants-2015_01