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HRID 863193作成日:2026年10月26日

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

https://huagongshe.com/reaction/863193

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物PhosphateHCID 1061—
反応物TriacetinHCID 5541—
反応物Sodium HydroxideHCID 14798—
反応物Methyl 6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058283—
溶媒tert-ButanolHCID 6386—
生成物(R)-6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 5135864741.4%

反応手順

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).

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-5c335ec9e1e64ec0999ed4ec547b1943
出典メモuspto-grants-1998_02