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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1899762Erstellt: 26. Oktober 2026

Hydrochloric Acid → 7-methoxy-1,2,3,4-tetrahydro-(2R)-2-naphthoic acid

https://huagongshe.com/reaction/1899762

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhosphateHCID 1061—
EduktTriacetinHCID 5541—
EduktSodium HydroxideHCID 14798—
EduktMethyl 7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058284—
LösungsmittelChloroformHCID 6212—
Lösungsmitteltert-ButanolHCID 6386—
Produkt7-methoxy-1,2,3,4-tetrahydro-(2R)-2-naphthoic acidHCID 14722818—

Reaktionsschritte

5 g (0.022 mol) of methyl 7-methoxy-1,2,3,4-tetrahydro-2-naphthoate are dissolved in 175 ml of tert-butanol, and 500 ml of phosphate buffer at pH 7 are added to the solution prepared in this way. The pH of the solution, which rises to a value of 7.3-7.5, is lowered to 7.1 by the addition of 1 N HCl. 3.5 g of Sigma PPL enzyme (known as porcine pancreatic lipase type II, crude, Sigma L-3126 - 39 U/mg using triacetin) are added to the mixture. The pH tends to drop as the reaction progresses, but is kept constant by the addition of a 0.25 N solution of NaOH. After 6 hours, when about 31.75 ml of 0.25 N NaOH have been consumed, sodium bicarbonate is added to the solution until the pH is about 8 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 5. The aqueous phase is acidified with concentrated sulfuric acid and the precipitate formed is filtered off to give 1.25 g of the title acid. [α]D20 =+43.67° (c=1.4%, CHCl3); ee 93.27% (HPLC performed under conditions (a)). This product is equivalent to that described in preparation (G) (i) of EP-A-436435, obtained after 10 crystallizations.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05573949
Quelldatensatzuspto-grants-1996_11
ORD IDord-9550397f0830484492386b9d40022bbf
Quellennotizuspto-grants-1996_11