Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58906949 | HCID 58906949 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58907104 | HCID 58907104 | 16.1% |
Reaction Steps
To a solution of example 94 (520 mg, 0.85 mmol) in EtOH (20 mL) was added 1N NaOH (2.5 mL, 3 eq.) and the reaction was stirred at 80° C. for 1 h. When all of the starting material had disappeared, the reaction cooled, evaporated to dryness, taken up with 1 N HCl and extracted with CH2Cl2. The organic phase was dried over Na2SO4, filtered and the solvent removed in vacuo. The residue was chromatographed eluting with CH2Cl2 (100%) then CH2Cl2/MeOH (95/5) to afford the title compound as a yellow oil (80 mg, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241793B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-90436345726f41cd920194c977e5abc1 |
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| Source note | uspto-grants-2007_07 |
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