戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 863197作成日:2026年10月27日

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

https://huagongshe.com/reaction/863197

反応式

関与物質

役割名称HCID仕込み量
反応物PhosphateHCID 1061—
反応物Sulfuric AcidHCID 1118—
反応物TriacetinHCID 5541—
反応物Sodium HydroxideHCID 14798—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058285—
溶媒tert-ButanolHCID 6386—
生成物5-Methoxy-1,2,3,4-tetrahydro-(2R)-2-naphthoic acidHCID 5445580216.2%

反応手順

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 0.25N 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°-152° C.; [α]D20 =+55.9° (c=1.4%, CHCl3); ee 85.6% (HPLC performed under conditions (e)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05719308
出典データセットuspto-grants-1998_02
ORD IDord-02e893b9e9aa4db9864ba8edda659b21
出典メモuspto-grants-1998_02