Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57941519 | HCID 57941519 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57941327 | HCID 57941327 | 64.2% |
Reaction Steps
A mixture of 2-((4S,7R)-1,7,8,8-tetramethyl-3-oxo-1,3,4,5,6,7-hexahydro-4,7-methano-indazol-2-ylmethyl)-benzoic acid methyl ester (304 mg, 0.86 mmol) and 1 M NaOH (1.5 mL, 1.5 mmol) in tetrahydrofuran (2.4 mL) and methanol (1.2 mL) was stirred overnight at room temperature. The reaction mixture was partitioned between water (100 mL) and ether (100 mL). The aqueous layer was acidified to pH<3 with 1 M HCl and the resulting mixture was extracted with chloroform (100 mL) and then chloroform containing a small amount of methanol (100 mL). The combined organic extracts were dried (magnesium sulfate), filtered, evaporated, and dried under vacuum to give 2-((4S,7R)-1,7,8,8-tetramethyl-3-oxo-1,3,4,5,6,7-hexahydro-4,7-methano-indazol-2-ylmethyl)-benzoic acid (188 mg, 64%) as an off-white solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622492B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-f0d88890427a49db9ba06a6155a4f5b7 |
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| Source note | uspto-grants-2009_11 |
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