HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 24753780, compound → HCID 11559437, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 24753780 | HCID 24753780 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 11559437 | HCID 11559437 | 97.9% |
Reaction Steps
Ethyl 6-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-2-pyridinecarboxylate (5.26 g, 13.8 mmol) was stirred at 60° C. for 2 hours in ethanol (15 ml) and 2M sodium hydroxide solution (5 mL). The reaction mixture was cooled and evaporated. The residue was diluted with water and extracted with diethyl ether. The aqueous phase was then acidified with glacial acetic acid and extracted with ethyl acetate (2×30 mL), dried (MgSO4) and evaporated to give the title compound as a yellow oil (4.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759369B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-fa28e4ff716e499290a93aec6764f77c |
| Source note | uspto-grants-2010_07 |