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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 863193생성일: 2026년 10월 25일

Hydrochloric Acid → (R)-6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

https://huagongshe.com/reaction/863193

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhosphateHCID 1061—
반응물TriacetinHCID 5541—
반응물Sodium HydroxideHCID 14798—
반응물Methyl 6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058283—
용매tert-ButanolHCID 6386—
생성물(R)-6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 5135864741.4%

반응 단계

3 g (0.0136 mol) of methyl 6-methoxy-1,2,3,4-tetrahydro-2-naphthoate are dissolved in 100 ml of tert-butanol, and 300 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. 1.5 g of Sigma PPL enzyme (known as porcine pancreatic lipase type II, crude, Sigma L-3126--50 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 0.25N solution of NaOH, the pH being controlled by an automatic titration apparatus. After 4-5 hours, when about 22 ml of 0.25N NaOH have been consumed, sodium bicarbonate is added to the solution until the pH is 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 2 below. The aqueous phase is acidified with concentrated sulfuric acid and the precipitate formed is filtered off to give 1.16 g of the title acid, which is crystallized from ethyl acetate. M.p. 130°-131° C.; [α]D20 =+57.8° (c=1.4%, CHCl3); ee 93.7% (HPLC performed under conditions (a)). This product is purer than that described in EP-A-436435, preparation (O) (i).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05719308
출처 데이터셋uspto-grants-1998_02
ORD IDord-5c335ec9e1e64ec0999ed4ec547b1943
출처 메모uspto-grants-1998_02