HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356722Generated: November 1, 2026
2-Mesitylenesulfonyl chloride → HCID 22731441, compound
https://huagongshe.com/reaction/1356722
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 3-methyl-1H-indole-5-carboxylate | HCID 12628587 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22731441 | HCID 22731441 | 90% |
Reaction Steps
To a solution of 5-carboethoxy-3-methylindole (601 mg, 2.96 mmol) in DMF, sodium hydride (178 mg, 4.45 mmol) and 2,4,6-trimethylbenzenesulfonyl chloride (971 mg, 4.44 mmol) were added under cooling with ice, followed by stirring for 30 min. The reaction mixture was mixed with a saturated aqueous NH4Cl solution, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine. The organic layer was dried over magnesium sulfate and evaporated under reduced pressure to remove the solvent; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:5) to give the titled compound (1.02 g, 90%). NMR (method a, CDCl3): δ 1.40 (3H, t, J=7.0 Hz), 2.29 (3H, s), 2.32 (3H, s), 2.52 (6H, s), 4.38 (2H, q, J=6.9 Hz), 6.95 (2H, s), 7.35 (1H, s), 7.41 (1H, d, J=8.9 Hz), 7.90 (1H, dd, J=1.4, 8.9 Hz), 8.24 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586630B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-05fa2f41682d47d080d7312dde8f61bf |
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| Source note | uspto-grants-2003_07 |
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