Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| Reactant | (+)-Methyl lactate | HCID 637514 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Product | HCID 129387551 | HCID 129387551 | — |
Reaction Steps
To a solution of 5.3 g (50.5 mmol) (R)-2-Hydroxy-propionic acid methyl ester in THF 50.5 mL (1 M in THF; 50.5 mmol) LiHMDS is added drop wise. After 10 minutes of stirring 4.0 g (25.2 mmol) 2-choro-3-nitro-pyridine is added. The mixture is stirred at 60° C. over night. The solvent is evaporated and the residue take up EtOAc washed with water, dried and evaporated to give rise to methyl (2R)-2-[(3-nitro-2-pyridyl)oxy]propanoate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09139577B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-21f718a9b9cc45639487e2af1f4f5ddf |
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| Source note | uspto-grants-2015_09 |
|---|