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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327348생성일: 2026년 10월 24일

Sodium Dithionite → 2,6-Dimethylhydroquinone

https://huagongshe.com/ko/reaction/327348

반응식

참여 물질

역할이름HCID투입량
반응물Sodium DithioniteHCID 24489—
반응물2,6-Dimethyl-1,4-benzoquinoneHCID 68241—
용매Diethyl EtherHCID 3283—
생성물2,6-DimethylhydroquinoneHCID 69560—

반응 단계

A solution of 2,6-dimethyl-1,4-benzoquinone (Xa) (5.66 g, 42 mmol, Aldrich) in Et2O (200 mL) was shaken vigorously in a separatory funnel with two 200 mL portions of aqueous sodium hydrosulfite solution (sodium dithionite, Na2S2O4, 14.5 g, 83.3 mmol) until the Et2O layer turned bright yellow. The ether layer was washed with brine (200 mL×2), dried (MgSO4) and concentrated in vacuo to obtain 4.865 g (35.3 mmol, Y: 83.9%) of the title compound as a white solid; mp, 148-150° C. (acetone-hexane) [mp reported by L. A. Carpino, S. A. Triolo, and R. A. Berglund in J. Org. Chem., 54, p. 3303 (1989): 145-148° C.]; Rf: 0.47 (10% EtOAc in CH2Cl2); IR(KBr) 3312 cm-1 (OH); 1H-NMR (300 MHz, acetone-d6) δ ppm: 2.15 (6H, s, Me), 6.45 (2H, s, Ar-H), 6.58 (1H, s, OH), 7.47 (1H, s, OH); 13C-NMR (75 MHz, acetone-d6) δ ppm: 16.84, 116.00, 126.45, 147.46, 151.54; MS (isobutane-DCI) m/e: 139 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05272171
출처 데이터셋uspto-grants-1993_12
ORD IDord-8134af87778846bd9cf68e5053a6503f
출처 메모uspto-grants-1993_12