HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725617Generated: November 1, 2026
Benzene → 4-Oxo-4-phenyl-2-[(trifluoroacetyl)amino]butanoic acid
https://huagongshe.com/reaction/1725617
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | 3-[(Trifluoroacetyl)amino]succinic anhydride | HCID 312805 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 4-Oxo-4-phenyl-2-[(trifluoroacetyl)amino]butanoic acid | HCID 569630 | — |
Reaction Steps
A solution of 3-[(trifluoroacetyl)amino]succinic anhydride (4.00 g, 19.0 mmol) and aluminum chloride (5.56 g, 41.7 mmol) in benzene (80 mL) was refluxed for 5 h, then cooled in an ice bath and quenched by the slow addition of water. The reaction mixture was worked up with ethyl acetate and 10% hydrochloric acid. The residue was purified by chromatography (silica gel, 100% methylene chloride to 90/10/1/1 methylene chloride/methanol/acetic acid/water gradient elution). Recrystallization of the resulting oil from methylene chloride/hexanes produced the title compound as a white solid (3.00 g). 1H NMR (500 MHz, (d6-acetone) □ 11.56 (bs, 1H), 8.63 (bs, 1H), 8.06 (dd, J=8.3, 1.2 Hz, 2H), 7.70-7.67 (m, 1H), 7.57 (t, J=7.7 Hz, 2H), 5.14-5.10 (m, 1H), 3.84 (dd, J=18.3, 6.8 Hz, 1H), 3.77 (dd, J=18.1, 4.6 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491713B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-9c331cb77223402aa2c088a6cfa95c7f |
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| Source note | uspto-grants-2009_02 |
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