HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872268Generated: October 31, 2026
Trifluoroacetic acid → HCID 18689623, compound
https://huagongshe.com/reaction/1872268
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 54573955 | HCID 54573955 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18689623 | HCID 18689623 | — |
Reaction Steps
A solution of 3-(hydroxy-phenyl-methyl)-1-(4-methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic acid benzhydryloxy-amide (5 mg, 0.008 mmoL) in dichloromethane (1 mL) was cooled to 0° C. This solution was treated with trifluoroacetic acid (0.1 mL) followed by a 0.31 M solution of triethylsilane in dichloromethane (0.026 mL). The reaction mixture was warmed from 0 to 25° C. over 35 minutes and then the solvents were removed in vacuo and the residue was coevaporated with toluene. The residue was purified by flash chromatography (silica, 5 to 10% methanol in dichloromethane) to give 3-(hydroxy-phenyl-methyl)-1(4-methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic acid hydroxyamide as a white solid; MS: (M-H)- 430.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06107291 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-514aecdcffaf478288c0c2424632ace0 |
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| Source note | uspto-grants-2000_08 |
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