Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl Glycolate | HCID 66774 | — |
| Reactant | HCID 178425983 | HCID 178425983 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18406865 | HCID 18406865 | 59% |
Reaction Steps
To a solution of 1-aminopyridin-2(1H)-iminium-2,4,6-trimethylbenzenesulfonate (1.24 g, 4 mmol) in EtOH (15 mL) was added NaOH (320 mg, 8 mmol). The mixture was heated to 60° C. and stirred for 1 h. Then methyl 2-hydroxyacetate (720 mg, 8 mmol) was added and the mixture was heated to 80° C. and stirred for 3 h. The resulting mixture was cooled to room temperature and concentrated under reduced pressure. The residue was washed with water (10 mL) and extracted with DCM (15 mL×3). The combined organic layers were washed with brine (10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the title compound as a pale yellow solid (350 mg, 59% yield). ESI MS: m/z 150 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249162B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-86cbdd96d5d74dc282c1334c1a472f30 |
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| Source note | uspto-grants-2016_02 |
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