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HRID 863196생성일: 2026년 10월 24일

Hydrochloric Acid → (R)-8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

https://huagongshe.com/ko/reaction/863196

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhosphateHCID 1061—
반응물TriacetinHCID 5541—
반응물Sodium HydroxideHCID 14798—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058286—
용매tert-ButanolHCID 6386—
생성물(R)-8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 756913243.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05719308
출처 데이터셋uspto-grants-1998_02
ORD IDord-afa3b577a7f84888a5d893d72db4aff1
출처 메모uspto-grants-1998_02