참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Acetamide, 2,2,2-trifluoro-N-(2-methylphenyl)- | HCID 137696 | — |
| 생성물 | 3-Methyl-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride | HCID 53627670 | 85% |
반응 단계
Synthesized according to general procedure 69. A mixture of 2,2,2-trifluoro-N-o-tolylacetamide (6.3 gm, 31 mmol) and chlorosulfonic acid (10.3 mL, 155 mmol) was heated at 155° C. for 15 min. After cooling to RT, the mixture was poured into ice water and extracted with EtOAc. The organic layer was concentrated and purified via silica gel chromatography using 0-25% EtOAc in hexanes gave 3-methyl-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride (7.8 g, 85%). 1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 7.53 (d, J=1.3 Hz, 1H), 7.46 (dd, J=8.1, 1.8 Hz, 1H), 7.21 (dd, J=8.1, 2.9 Hz, 1H), 2.18 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08309587B2 |
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| 출처 데이터셋 | uspto-grants-2012_11 |
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| ORD ID | ord-e6834bc6d0e24ea685fa55c458765996 |
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| 출처 메모 | uspto-grants-2012_11 |
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