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HRID 465766作成日:2026年10月25日

Water → 2,3-Dicarbomethoxycyclobutyl phenyl sulfone

https://huagongshe.com/reaction/465766

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1,2-DichloroethaneHCID 11—
溶媒MethanolHCID 887—
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) δ 2.48 (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US05153352
出典データセットuspto-grants-1992_10
ORD IDord-b7f098d2a9c948eaaf89405774fe2358
出典メモuspto-grants-1992_10