참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Sulfate | HCID 24507 | — |
| 반응물 | Dimethyl 3-(phenylthio)cyclobutane-1,2-dicarboxylate | HCID 19794294 | — |
| 반응물 | Potassium hydroxy sulfite | HCID 23707502 | — |
| 반응물 | Potassium peroxymonosulfate | HCID 23712892 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2,3-Dicarbomethoxycyclobutyl phenyl sulfone | HCID 19794268 | 94% |
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) 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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05153352 |
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| 출처 데이터셋 | uspto-grants-1992_10 |
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| ORD ID | ord-b7f098d2a9c948eaaf89405774fe2358 |
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| 출처 메모 | uspto-grants-1992_10 |
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