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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 856946생성일: 2026년 10월 25일

Water → 3-Hydroxy-8-oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrile

https://huagongshe.com/reaction/856946

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물5,6,7,8-Tetrahydro-2-naphtholHCID 14305—
용매1,4-DioxaneHCID 31275—
생성물3-Hydroxy-8-oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 2186496440%

반응 단계

5,6,7,8-tetrahydro-2-naphthalenol prepared in method II-2 (1.5 g, 8.7 mmol) was dissolved in 1,4-dioxane (8 mL) in a 100 mL round bottom flask. To this was added water (2 mL), and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) (4.1 g, 18.2 mmol, 2.1 eq) in anhydrous 1,4-dioxane (16 mL) dropwise. The reaction mixture turned to black immediately after addition and resulting mixture was stirred at room temperature for 3 h. The mixture was filtered and the filtrate was evaporated in vacuo. The residue was participated between EtOAc and saturated aqueous sodium bicarbonate. The aqueous layer was acidified to about pH 3 and was extracted with EtOAc three times. The organic layers were combined and evaporated in vacuo. Purification using MPLC chromatography (Biotage) gave 0.64 g (40%) of 3-hydroxy-8-oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrile as a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07144885B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-461f0709edcb44938e20f19979f597a7
출처 메모uspto-grants-2006_12