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HRID 483713作成日:2026年10月23日

2,3-Dihydroxybutanedioic Acid → 4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether

https://huagongshe.com/ja/reaction/483713

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dihydroxybutanedioic AcidHCID 875—
反応物Sodium SulfateHCID 24436—
反応物4-Cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl etherHCID 14850577—
反応物DiisobutylaluminumhydrideHCID 21225700—
溶媒Diethyl EtherHCID 3283—
生成物4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl etherHCID 14850579—

反応条件

温度25 °C

反応手順

15.5 ml (19.7 mmol) of diisobutylaluminum hydride solution (20% in hexane) were added dropwise under nitrogen to a solution of 3 g (9.4 mmol) of 4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether in 40 ml of dry ether at 25° C. The mixture was stirred at 25° C. for 40 min and then 250 ml of saturated tartaric acid solution were added dropwise. Subsequently, a little sodium sulfate solution was added, and the phases were separated. The aqueous phase was extracted with ether, and the organic extract was washed with saturated tartaric acid solution and water, dried over Na2SO4 and concentrated. Recrystallization from methanol resulted in 1.4 g of the title compound of melting point 102°-104° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05225601
出典データセットuspto-grants-1993_07
ORD IDord-3a18719b85964a5597bd3a8d2ad76551
出典メモuspto-grants-1993_07