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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485233Generated: October 31, 2026

Toluene → Ethyl 2-(3-chloropyrazin-2-yl)acetate

https://huagongshe.com/reaction/1485233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
Reactant2,3-DichloropyrazineHCID 78575—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventAmmonium ChlorideHCID 25517—
ProductEthyl 2-(3-chloropyrazin-2-yl)acetateHCID 5341938531%

Reaction Steps

To a 1.0 M solution of LiHMDS in toluene (14.8 mL, 14.8 mmol) under nitrogen at 0° C. was added 2,3-dichloropyrazine (0.699 mL, 6.71 mmol) and ethyl acetate (0.725 mL, 7.38 mmol). The mixture was stirred overnight for 18 hours, allowing the ice bath to warm to room temperature. The mixture was poured into saturated ammonium chloride (100 mL), and extracted with diethyl ether (3×100 mL). The combined ether extracts were washed with brine, dried (sodium sulphate) and evaporated. The residue was chromatographed (40 g silica cartridge, 0-25% ethyl acetate/petroleum benzine 40-60° C.) to give the title compound (I99) (0.414 g, 31% yield) as a pale yellow oil; 1H NMR (400 MHz, CDCl3) δ 8.46 (d, J=2.5 Hz, 1H), 8.31 (d, J=2.5 Hz, 1H), 4.22 (q, J=7.1 Hz, 2H), 4.03 (s, 2H), 1.27 (t, J=7.1 Hz, 3H). LCMS Method C: rt 5.16 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09421205B2
Source datasetuspto-grants-2016_08
ORD IDord-581a3c18320d41769c6aa306aa1fddef
Source noteuspto-grants-2016_08