HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054605Generated: November 4, 2026
Trifluoroacetic acid → HCID 59655970, compound
https://huagongshe.com/reaction/2054605
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131726763 | HCID 131726763 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59655970 | HCID 59655970 | 100% |
Reaction Steps
Trifluoroacetic acid (0.5 mL) was added to a solution of 4-(4′-Dibenzofuran-4-ylbiphen-4-ylmethyl)-piperazine-1,2-dicarboxylic acid, 1-tert-butyl ester (80 mg) in anhydrous dichloromethane. The reaction was stirred at room temperature for 2 hours (TLC control). The resultant brown oil was reconstituted and concentrated from methanol (3×10 mL) and then from dichloromethane (2×10 mL) to give the title compound as a white solid (65 mg, 100%): Rf 0.25 (20% methanol in dichloromethane). 1H NMR (DMSO-d6, 300 MHz): δ 8.19 (1H, d, J=9 Hz, Ar—H), 8.16 (1H, d, J=9 Hz, Ar—H), 8.01 (2H, d, J=9 Hz, Ar—H), 7.86 (2H, d, J=9 Hz, Ar—H), 7.72 (4H, m, Ar—H), 7.53 (2H, q, J=8 Hz, Ar—H), 7.45 (3H, m, Ar—H), 4.22 (1H, m, CHN), 3.78 (2H, s), 3.35 (1H, m), 3.08 (2H, m), 2.86 (1H, m), 2.58 (2H, m); ESI-LCMS e/z calcd for C30H26N2O3 462.546, found 563 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329680B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-1a454e444d7f4ad38afa3e4d9a71f61c |
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| Source note | uspto-grants-2008_02 |
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