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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471718Generated: October 30, 2026

Methyl chloroformate → (3-Chloropyrazin-2-yl)methanol

https://huagongshe.com/reaction/1471718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant3-Chloro-2-pyrazine-carboxylic acidHCID 1501900—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3-Chloropyrazin-2-yl)methanolHCID 4015221322%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-chloropyrazine-2-carboxylic acid (2.0 g, 12.70 mmol, 1.0 eq.) and TEA (3.50 mL, 25.40 mmol, 2.0 eq.) in THF (50 mL) was added methyl chloroformate (1.2 mL, 15.20 mmol, 1.2 eq.) at 0° C. The mixture was stirred at 0° C. for 10 min and filtered. To this filtrate was added a suspension of NaBH4 (0.97 g, 25.40 mmol, 2 eq.) in water (1.0 mL) at 0° C. The mixture was stirred at 0° C. for 1 h, quenched with NH4Cl(aq) solution, and extracted with EtOAc twice. The combined organic layers were dried over Na2SO4, concentrated, and purified on silica gel using a mixture of EtOAc and hexanes as eluent to give (3-chloropyrazin-2-yl)methanol (400 mg, 22%) as a white solid. 1H NMR (400 MHz, MeOD) δ 8.58 (d, J=2.5 Hz, 1H), 8.38 (d, J=2.5 Hz, 1H), 4.84 (s, 2H). LRMS (M+H+) m/z 145.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012450B2
Source datasetuspto-grants-2015_04
ORD IDord-2b11664989d24ded85fd1d515b5d0831
Source noteuspto-grants-2015_04