HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 553571Erstellt: 24. Oktober 2026
Sodium Hydroxide → (1R,3S)-2-Methyl-6-{2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxy]ethoxy}benzoic acid
https://huagongshe.com/de/reaction/553571
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Ethyl (1R,3S)-2-methyl-6-{2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)-cyclohexyloxy]ethoxy}benzoate | HCID 59820046 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Produkt | (1R,3S)-2-Methyl-6-{2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxy]ethoxy}benzoic acid | HCID 59820060 | — |
Reaktionsschritte
Unpurified ethyl (1R,3S)-2-methyl-6-{2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxy]ethoxy}benzoate are dissolved in 3 ml of methanol, and 0.25 ml of a 5 N sodium hydroxide solution are added. The mixture is stirred at 60° C. for 8 h and at 80° C. for 12 h. After cooling, the mixture is taken up in 2N HCl/ethyl acetate, the organic phase is dried over sodium sulfate and the solvent is removed under reduced pressure. The residue is purified by RP-HPLC. This gives (1R,3S)-2-methyl-6-{2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxy]ethoxy)benzoic acid as a colorless oil. C28H33NO6 (479.58), MS (ESI). 480 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08048901B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-be0d8dec52454863864b00770e568257 |
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| Quellennotiz | uspto-grants-2011_11 |
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