참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-acetyl-o-toluidine | HCID 8443 | — |
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | 2-methoxy-N-phenylacetamide | HCID 264222 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 3-Acetamido-4-methylbenzene-1-sulfonyl chloride | HCID 54594388 | — |
반응 단계
Chlorosulfonic acid (500 g.) was taken in a three neck round bottom flask equipped with a guard tube and cooled it to 10° C. N-acetyl 2-toluidine (100 g.) was added in small portions maintaining temperature below 10° C. After complete addition of 2-methoxy acetanilide cooling is removed and reaction was brought to 25° C. Reaction mixture was stirred at 25° C. for further 24 hours. After the completion of reaction (TLC), the reaction mixture was poured on ice-water, and the resulting slurry was filtered on buchner funnel. Solid cake on funnel was washed with 500 mL of water and the resulting solid was dried on phosphorus pentoxide in a desiccator to obtain 113.5 grams off white solid. It was found to contain a mixture of two isomers as confirmed from NMR and HPLC; however the desired isomer was obtained by partial crystallization using benzene and used for further experimentation, after the thorough carectorisation.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07998981B2 |
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| 출처 데이터셋 | uspto-grants-2011_08 |
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| ORD ID | ord-93c966f566a443cc85f54105e5a872b4 |
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| 출처 메모 | uspto-grants-2011_08 |
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