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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1899766생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1899766

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—
반응물(S)-Methyl 8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 22866791—
용매tert-ButanolHCID 6386—
생성물(R)-8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 7569132—

반응 단계

1.1 g (0.0051 mol) of methyl 8-methoxy-1,2,3,4-tetrahydro-2-naphthoate are dissolved in 39 ml of tert-butanol, and 112 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 1 N HCl. 1.25 g of Sigma PPL enzyme (known as porcine pancreatic lipase type II, crude, Sigma L-3126 - 46 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, the pH being controlled by an automatic titration apparatus. After 7 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. 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 0.42 g of the title acid. ee 98% (HPLC performed under conditions (d)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05573949
출처 데이터셋uspto-grants-1996_11
ORD IDord-ef2c2bfd9ff448d69f04756872f49a2a
출처 메모uspto-grants-1996_11