Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58677833 | HCID 58677833 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21100220 | HCID 21100220 | 40% |
Reaction Steps
To 6.51 mmol 2-cyclobutylmethoxy-5-methanesulfonyl-benzoic acid methyl ester in 20 ml tetrahydrofuran was added 40 mmol 2 N aq NaOH solution and the reaction mixture was stirred at 60° C. for 2 hours. After such time the reaction mixture was acidified by addition of concentrated HCl and extracted twice with dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. The residue was triturated in ether to give the title compound as a white solid (40% over 2 steps). MS (m/e): 283.3 ([M−H]−, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220744B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-0a6aca494db149379d34d017a330437d |
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| Source note | uspto-grants-2007_05 |
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