HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-(4-Hydroxyphenyl)-4,4-dimethoxy butyric acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | 4-Oxo-3-[4-(tetrahydropyran-2-yloxy)-phenyl]-butyric acid methyl ester | HCID 57771437 | — |
| Product | 3-(4-Hydroxyphenyl)-4,4-dimethoxy butyric acid methyl ester | HCID 57771503 | — |
Reaction Steps
To a solution of 4-oxo-3-[4-(tetrahydropyran-2-yloxy)-phenyl]-butyric acid methyl ester (1.29 g) obtained in Step 3 in methanol (13 mL) was added camphorsulfonic acid (98 mg), followed by stirring the reaction mixture at room temperature for 6 hours. Then, after addition of 1N aqueous sodium hydroxide solution (0.42 mL), the reaction mixture was concentrated. To the residue was added water, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, dried and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:2 to 2:3) to give 3-(4-hydroxyphenyl)-4,4-dimethoxy butyric acid methyl ester (0.99 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299296B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-1a816049059c46fbb238a5ed2dfcd97a |
| Source note | uspto-grants-2012_10 |