참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Ethyl anisate | HCID 60979 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | Ethyl 3-chlorosulfanyl-4-methoxybenzoate | HCID 86760945 | — |
반응 단계
A solution of ethyl 4-methoxybenzoate (15.7 g; 87.2 mmol) in CCl4 (60 ml) was cooled to −15° C., and chlorosulfonic acid (17.5 ml; 263 mmol) was added dropwise over a period of 15 min, resulting in a temperature increase to −10° C. After the addition had ended, the reaction mixture was stirred at room temperature for 2 h and then heated at 50° C. until no more starting material could be detected by thin-layer chromatography. With ice-cooling and vigorous stirring, the reaction mixture was added to a suspension of ice (50 g) in CCl4 (100 ml). The mixture was stirred vigorously for 3 min. The organic phase was separated off and the aqueous phase was extracted with CH2Cl2 (3×100 ml). The combined organic extracts were washed with saturated NaCl solution (3×), dried over Na2SO4 and concentrated. Trituration of the oily brown residue with diethyl ether resulted in 5c precipitating as a crystalline white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07582660B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-8b1f4730d34648b9b5b1ba32c747ea69 |
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| 출처 메모 | uspto-grants-2009_09 |
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