Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22036247 | HCID 22036247 | 75% |
Reaction Steps
A mixture of 3-bromophenol (173 g. 100 mmol), ethylene oxide (0 44 g, 10 mmol), Et3N (3 drops) and dioxane (4 mL) was heated at 100° C. in a sealed tube for 2 d. The solution was cooled in an ice-bath and KO-t-Bu (1.07 g, 9.50 mmol) followed by 2,3-dichloropyrazine (1.34 g, 9 mmol) were added along with dioxane (1 mL). The mixture was stirred at room temperature for 90 min, diluted with CH2Cl2 and filtered. The filtrate was concentrated and the residue was purified by chromatography on silica gel (gradient: isohexane to 25% EtOAc/isohexane) to give 2.21 g (75%) of the title product as a white solid: mp 57-58° C. Anal. (C12H10BrClN2O2) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534794B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-412e29f45fac4f7a832b7fff08d59d45 |
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| Source note | uspto-grants-2009_05 |
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