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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1899765생성일: 2026년 10월 25일

Phosphate → 5-Methoxy-1,2,3,4-tetrahydro-(2R)-2-naphthoic acid

https://huagongshe.com/reaction/1899765

반응식

참여 물질

역할이름HCID투입량
반응물PhosphateHCID 1061—
반응물Sulfuric AcidHCID 1118—
반응물TriacetinHCID 5541—
반응물Sodium HydroxideHCID 14798—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058285—
용매tert-ButanolHCID 6386—
생성물5-Methoxy-1,2,3,4-tetrahydro-(2R)-2-naphthoic acidHCID 5445580216.2%

반응 단계

0.8 g (0.0036 mol) of methyl 5-methoxy-1,2,3,4-tetrahydro-2-naphthoate is dissolved in 28 ml of tert-butanol, and 80 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 dilute H2SO4. 0.450 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 0.25 N solution of NaOH, the pH being controlled by an automatic titration apparatus. After 8 hours, sodium bicarbonate is added to the solution until the pH is 7.7 in order to stop the reaction by inactivation of the enzyme. Extraction is carried out with isopropyl ether and the two phases are separated. The organic phase contains the unreacted ester principally of (S) configuration. The aqueous phase is acidified with concentrated sulfuric acid and extracted with ethyl ether, the organic phase is dried over sodium sulfate and the solvent is evaporated off under reduced pressure. The product obtained is crystallized from isopropyl ether to give 0.12 g of the title compound. M.p. 150°-15° C.; [α]D20 =+55.9° (c=1.4%, CHCl3); ee 85.6% (HPLC performed under conditions (e)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05573949
출처 데이터셋uspto-grants-1996_11
ORD IDord-e3307e94f6b947eb896b5ac70a688682
출처 메모uspto-grants-1996_11