HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289449Generated: October 30, 2026
Trifluoroacetic acid → HCID 20077199, compound
https://huagongshe.com/reaction/1289449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20077201 | HCID 20077201 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20077199 | HCID 20077199 | 88% |
Reaction Steps
Dissolved in 6 ml of methylene chloride were 1.77 g (5.00 mmol) of ethyl [2-(t-butoxycarbonylaminomethyl)indane-5-oxy]acetate, and 4 ml of trifluoroacetic acid were added under chilling with ice water, followed by stirring for 1 hour. The liquid reaction mixture was diluted with 40 ml of methylene chloride, and a solution of 8.37 g (60 mmol) of potassium carbonate in 40 ml of water was added, followed by vigorous stirring. After 10 minutes, 1.07 g (6.00 mmol) of phenyl-sulfonyl chloride were added, and the resultant mixture was stirred further for 1.5 hours. An organic layer separated was taken out, dried and then concentrated, and the residue was purified by column chromatography on silica gel (ethyl acetate: hexane=1:1), thereby obtaining 1.68 g of a colorless oily substance. Yield: 88%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750524 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-de1270c980db4fe986c4d826d0e82fce |
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| Source note | uspto-grants-1998_05 |
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