돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 863194생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/863194

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhosphateHCID 1061—
반응물TriacetinHCID 5541—
반응물Sodium HydroxideHCID 14798—
반응물Methyl 7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058284—
용매ChloroformHCID 6212—
용매tert-ButanolHCID 6386—
생성물7-methoxy-1,2,3,4-tetrahydro-(2R)-2-naphthoic acidHCID 14722818—

반응 단계

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 1N 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 0.25N solution of NaOH. After 6 hours, when about 31.75 ml of 0.25N 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05719308
출처 데이터셋uspto-grants-1998_02
ORD IDord-4b0311a0527b4a9fb76d079b73df33f5
출처 메모uspto-grants-1998_02