HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272869Generated: October 31, 2026
Chloroacetaldehyde → HCID 117874517, compound
https://huagongshe.com/reaction/2272869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 2-pyrazineacetate | HCID 1514203 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 117874517 | HCID 117874517 | — |
Reaction Steps
To a solution of 10 g (65.7 mmol) of methyl pyrazin-2-ylacetate in 263 mL of anhydrous acetone (4 mL/mmol) there are added in succession 5.7 g of lithium bromide (65.7 mmol), 22.1 g of sodium bicarbonate (263 mmol) and then 9.4 mL of chloroacetaldehyde (50% solution in water) (72.6 mmoles). The whole is subsequently heated at reflux overnight. The reaction mixture is subsequently concentrated to dryness and then taken up in ethyl acetate. The organic phase is washed with a saturated sodium chloride solution, dried over magnesium sulphate, filtered and then concentrated to dryness. There is obtained an oil, which is purified by chromatography over silica gel (CH2Cl2/ethyl acetate gradient). After concentration, the title product is obtained in the form of a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120791B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-21fac2efb26943c98ae8dc423de42668 |
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| Source note | uspto-grants-2015_09 |
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