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HRID 863196Erstellt: 23. Oktober 2026
Hydrochloric Acid → (R)-8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
https://huagongshe.com/de/reaction/863196
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Phosphate | HCID 1061 | — |
| Edukt | Triacetin | HCID 5541 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Methyl 8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate | HCID 13058286 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | (R)-8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid | HCID 7569132 | 43,2% |
Reaktionsschritte
0.743 g (0.0034 mol) of methyl 8-methoxy-1,2,3,4-tetrahydro-2-naphthoate is dissolved in 26 ml of tert-butanol, and 75 ml of phosphate buffer at pH 7 are added to the solution prepared in this way. The pH of the solution, which rises to 7.3-7.5, is lowered to 7.1 by the addition of 1N HCl. 0.836 g of Sigma PPL enzyme (known as porcine pancreatic lipase type II, crude, Sigma L-3126--46 U/mg using triacetin) is added to the mixture. The pH tends to drop as the reaction progresses, but is kept constant by the addition of a 0.25N solution of NaOH, the pH being controlled by an automatic titration apparatus. After 6.5 hours, the mixture is poured into a 5% solution of sodium bicarbonate in order to stop the reaction by inactivation of the enzyme. Extraction is carried out with ethyl ether and the two phases are separated. The organic phase contains the unreacted ester principally of (S) configuration, which can be recovered as indicated in Example 10 below. The aqueous phase is acidified with 10% sulfuric acid and extracted with chloroform; the organic phase is filtered on Celite and dried over sodium sulfate and the solvent is evaporated off under reduced pressure to give 0.303 g of the title acid, which is crystallized from isopropyl ether. ee 95.2% (HPLC performed under conditions (d)); m.p. 137°-138° C.; [α]D25 =+54.6° (c=1.4%, CH3OH).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05719308 |
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| Quelldatensatz | uspto-grants-1998_02 |
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| ORD ID | ord-afa3b577a7f84888a5d893d72db4aff1 |
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| Quellennotiz | uspto-grants-1998_02 |
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