HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 12-(3-Chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)dodecanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 12-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)dodecanate | HCID 87428760 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 12-(3-Chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)dodecanoic acid | HCID 87428873 | — |
Reaction Steps
NaOH (21 mg, 0.48 mmol) was added to a mixed solution of 215-15-COOEt (101 mg, 0.246 mmol) in acetone (1.3 ml)/H2O (0.7 ml) at room temperature followed by stirring for 12 hours. After dilution of the reaction solution with EtOAc, the diluted solution was acidified with a 1 M aqueous HCl solution. After addition of a saturated aqueous NaCl solution, the organic layer was separated. The aqueous layer was then extracted with EtOAc twice, and the combined organic layer was dried over Na2SO4. After evaporation of the solvent, the residue was purified by column chromatography on silica gel (Hexane:EtOAc=2:1) to yield the target product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440913B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-cb01281cf78a4835bda1ca8a36e8c9da |
| Source note | uspto-grants-2016_09 |