HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355702Generated: October 29, 2026
Tetrahydrofuran → HCID 21714327, compound
https://huagongshe.com/reaction/355702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 21714308 | HCID 21714308 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21714327 | HCID 21714327 | — |
Reaction Steps
A mixture of ethyl 7-[N-methyl-N-(2-hydroxyethyl) amino]-4-trifluoromethyl-1H-indole-2-carboxylate (0.37 g, 1.12 mmol), triethylamine (0.25 g, 2.46 mmol) and tetrahydrofuran (20 ml) was cooled to -19° C., after which methanesulfonyl chloride (0.14 g, 1.23 mmol) was added dropwise with stirring. The reaction mixture was stirred at -18° C. to -13° C. for 1 hour, poured into cold water, and then extracted three times with ethyl acetate. The extract solution was washed with a 5% aqueous sodium hydrogencarbonate solution and a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain an oil of ethyl 7-[N-methyl-N-(2-methanesulfonyloxyethyl)amino]-4-trifluoromethyl-1H-indole-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834454 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-5f89256dbd454e5dbdc6d0fe54e99975 |
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| Source note | uspto-grants-1998_11 |
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