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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483713생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dihydroxybutanedioic AcidHCID 875—
반응물Sodium SulfateHCID 24436—
반응물4-Cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl etherHCID 14850577—
반응물DiisobutylaluminumhydrideHCID 21225700—
용매Diethyl EtherHCID 3283—
생성물4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl etherHCID 14850579—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05225601
출처 데이터셋uspto-grants-1993_07
ORD IDord-3a18719b85964a5597bd3a8d2ad76551
출처 메모uspto-grants-1993_07