HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229760Generated: November 3, 2026
Methanesulfonyl chloride → HCID 18675452, compound
https://huagongshe.com/reaction/2229760
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18675457 | HCID 18675457 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18675452 | HCID 18675452 | — |
Reaction Steps
To a solution of 3-(3-chlorophenyl)indoline (3.88 g, 16.9 mmol) and DIEA (2.40 g, 18.6 mmol) in DCM (40 mL) was added dropwise methanesulfonyl chloride (2.13 g, 18.6 mmol) at about 0° C. The mixture was stirred for about 1.5 hours. The solution was diluted with DCM and washed with saturated NaHCO3 solution (2 times), 1N HCl aqueous solution (2 times) and brine (2 times) and dried over anhydrous MgSO4, filtered and concentrated in vacuo. The crude product was purified by column chromatography on silica, eluting with EtOAc/hexane 1:4. The title compound was obtained as an oil Yield: 4.40 9, 85%. Rf=0.41, silica, EtOAc/hexane 1:2. 1H NMR (300 MHz, CDCl3) δ:7.52 (d, 1H), 7.24-7.34 (m, 3H), 7.20 (s, 1H), 7.02-7.14 (m, 3H), 4.59 (t, 1H), 4.38 (t, 1H), 3.87 (dd, 1H), 2.92 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420555B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-49e8a3091d434bc2b6489aaf40cd50b3 |
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| Source note | uspto-grants-2002_07 |
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