HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715973Generated: October 25, 2026
Chlorosulfonic acid → 3-Methyl-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride
https://huagongshe.com/reaction/1715973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Acetamide, 2,2,2-trifluoro-N-(2-methylphenyl)- | HCID 137696 | — |
| Product | 3-Methyl-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride | HCID 53627670 | 85% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799822B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-23a7bda2142c48c18dff63eb5027a22f |
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| Source note | uspto-grants-2010_09 |
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