HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 90950016, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 23134229 | HCID 23134229 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 90950016 | HCID 90950016 | 43.3% |
Reaction Steps
Lead tetraacetate (1.369 g) was added to an ice-cooled mixture of 1-[4′-(2-acetoxyethoxy)-2′,6′-dimethylbiphenyl-4-yl]ethan-1-one (0.672 g), boron trifluoride diethyl etherate (1.56 mL), methanol (2 mL) and methylene chloride (20 mL) with stirring, and the mixture was stirred at room temperature for 4 hrs. Water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/2) to afford methyl[4′-(2-acetoxyethoxy)-2′,6′-dimethylbiphenyl-4-yl]acetate (0.318 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417169B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-9e4945db30ad48fdb0d6cf896114bd8d |
| Source note | uspto-grants-2008_08 |