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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | Ethyl 2-(3-chloropyrazin-2-yl)acetate | HCID 53419385 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09421205B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-581a3c18320d41769c6aa306aa1fddef |
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| Source note | uspto-grants-2016_08 |
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