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HRID 1899764作成日:2026年10月27日

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

https://huagongshe.com/reaction/1899764

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Sodium BicarbonateHCID 516892—
反応物Methyl 8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058286—
溶媒tert-ButanolHCID 6386—
生成物(R)-8-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 756913243.2%

反応手順

0.743 g (0.0034 mol) of methyl 8-methoxy-1,2,3,4-tetrahydro-2-naphthoate is dissolved in 26 ml of tert-butanol, and 75 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. 0.836 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 0.25 N solution of NaOH, the pH being controlled by an automatic titration apparatus. After 6.5 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 as indicated in Example 10 below. 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 0.303 g of the title acid, which is crystallized from isopropyl ether. ee 95.2% (HPLC performed under conditions (d)); m.p. 137°-138° C.; [α]D25 =+54.6° (c=1.4%, CH3OH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05573949
出典データセットuspto-grants-1996_11
ORD IDord-142ad68d0d7d4242b72076f03b535e38
出典メモuspto-grants-1996_11