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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5973생성일: 2026년 10월 24일

Water → 2,3-Dicarbomethoxycyclobutyl phenyl sulfone

https://huagongshe.com/ko/reaction/5973

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium SulfateHCID 24507—
반응물Dimethyl 3-(phenylthio)cyclobutane-1,2-dicarboxylateHCID 19794294—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물Potassium peroxymonosulfateHCID 23712892—
용매MethanolHCID 887—
용매1,1-DichloroethaneHCID 6365—
생성물2,3-Dicarbomethoxycyclobutyl phenyl sulfoneHCID 1979426894%

반응 단계

To a vigorously stirred solution of 1.05 g (3.75 mmol) of dimethyl 3-(phenylthio)cyclobutane-1,2-dicarboxylate from Step A in 20 mL of methanol, was added slowly a suspension of 3.46 g (11.25 mmol) of OXONE (a commercially available mixture of sulfuric acid potassium salt and potassium hydrogen peroxymonosulfate) in 20 mL of water. The resultant cloudy suspension was stirred for 0.5 h then diluted with 50 mL of water and 100 mL of 1,2=dichloroethane. The phases were allowed to separate and the aqueous phase was extracted with 20 mL of 1,2-dichloroethane. The combined organic layers were washed with 2×50 mL of dilute aqueous sodium bicarbonate solution, 2×50 mL of water and 50 mL of brine, dried over anhydrous magnesium sulfate and concentrated to give 1.10 g (94% yield) of the title compound as a viscous oil; EI-MS, m/e (relative intensity): 281 (M+ --OCH3, 9), 171 (100), 139 (24), 111 (47); 1H NMR (CDCl3) δ2.48 (m, 1H), 2.76 (m, 1H), 3.23 (q, 1H), 3.52 (s, 3H), 3.74 (s, 3H), 3.80 (m, 1H), 3.92 (q, 1H), 7.58 (m, 2H), 7.68 (m, 1H), 7.89 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246931
출처 데이터셋uspto-grants-1993_09
ORD IDord-70dbc0e828674b098de600e6c942e203
출처 메모uspto-grants-1993_09