HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 58612420, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58612418 | HCID 58612418 | — |
| Catalyst | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 58612420 | HCID 58612420 | 485.3% |
Reaction Steps
Methanol (1.4 mL), and trimethyl orthoformate (1.79 g, 16.95 mmol) were added to 1-(3-tert-butyl-5-chloro-4-methoxyphenyl)ethanone (1.36 g, 5.65 mmol), followed by stirring at room temperature. In addition, (±)-10-camphorsulfonic acid [(±)-CSA] (65 mg, 0.282 mmol, 5 mol %) was added, followed by 2 hours of stirring. Potassium carbonate (156 mg, 1.128 mmol) was added. After 40 minutes of stirring, water (10 mL) and n-heptane (10 mL) were added, and the solution was separated. After washing the organic layer with water (10 mL), the solvent was evaporated (50° C.) to obtain 1.57 g of the subject compound as a yellow oily substance (yield: 96.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375236B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-9135e33491574fbeabf2c44b9e913f04 |
| Source note | uspto-grants-2008_05 |