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HRID 5973作成日:2026年10月24日

Water → 2,3-Dicarbomethoxycyclobutyl phenyl sulfone

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium SulfateHCID 24507—
反応物Dimethyl 3-(phenylthio)cyclobutane-1,2-dicarboxylateHCID 19794294—
反応物Potassium hydroxy sulfiteHCID 23707502—
反応物Potassium peroxymonosulfateHCID 23712892—
溶媒MethanolHCID 887—
溶媒1,1-DichloroethaneHCID 6365—
生成物2,3-Dicarbomethoxycyclobutyl phenyl sulfoneHCID 1979426894%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246931
出典データセットuspto-grants-1993_09
ORD IDord-70dbc0e828674b098de600e6c942e203
出典メモuspto-grants-1993_09