Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 57545214 | HCID 57545214 | — |
| Reactant | HCID 178502572 | HCID 178502572 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68998580 | HCID 68998580 | — |
Reaction Steps
A mixture of 500 mg (1.08 mmol) of (3S*,3aR*,8bR*)-3a-(4-chlorophenyl)-6,8-diethoxy-8b-hydroxy-3-phenyl-2,3,3a,8b-tetrahydrocyclopenta[b]benzofuran-1-one (Example 15A) and 1.08 ml (2.15 mmol) of a 2 M solution of methoxymagnesium methyl carbonate in DMF is heated with stirring at 100° C. in a closed vessel for 16 h. The resulting suspension is then poured into a mixture of ice-cold 5 N hydrochloric acid and ethyl acetate. The organic phase is separated off, washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered with suction and concentrated. 531 mg of crude product are employed directly in the next stage without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030347B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c9e4a6358c964ec8a9e3705d4a08f25f |
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| Source note | uspto-grants-2011_10 |
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