Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178437623 | HCID 178437623 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14881217 | HCID 14881217 | 78.5% |
Reaction Steps
Ethylene chlorohydrin (32.21 g, 0.4M) was added to a solution of 2-hydroxy-3-ethyl-5,6-dimethyl-pyrazine (12.16 g, 80 mM) and 5N NaOH (80 ml) in t-butanol (240 ml), and stirred at 60° C. for 3 hours. Dilute aqueous K2CO3 was added to the reaction mixture, the mixture extracted with chloroform, and the resultant aqueous layer extracted twice with further chloroform. The combined chloroform layers were dried with anhydrous magnesium sulfate and concentrated in vacuo. The residue was charged on a column of silica-gel (C-200, 250 g) packed with chloroform and eluted with chloroform-methanol form-methanol (from 200:1 to 50:1) to obtain compound 630 (12.31 g, yield: 78.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837319 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-b22c1990747d4a368021e38be49fad4a |
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| Source note | uspto-grants-1989_06 |
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