HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Methanesulfonyl-6-nitroindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Nitroindoline | HCID 29757 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methanesulfonyl-6-nitroindoline | HCID 23112213 | 95.4% |
Reaction Steps
In 50 ml of methylene chloride was dissolved 2.5 g of 6-nitroindoline, and then 6.37 ml of triethylamine was added thereto. Under ice cooling, 3.51 g of methanesulfonyl chloride was added dropwise, the reaction solution was stirred at room temperature for 3 hours, and then ice-water was added thereto, followed by 1 hour of stirring. The reaction solvent was removed by evaporation under reduced pressure, a 1M aqueous hydrochloric acid solution was added to the residue, and precipitated was filtrated off, whereby 3.52 g of 1-methylsulfonyl-6-nitroindoline was obtained as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585878B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-7eb762482f7e4844b54ede913f762c9d |
| Source note | uspto-grants-2009_09 |