HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062385Generated: October 26, 2026
Aniline → (R)-N-[2-Chloro-4-(N-phenylcarbamoyl)phenyl]-2-hydroxy-2methyl-3,3,3-trifluoropropanamide
https://huagongshe.com/reaction/1062385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (R)-N-(2-chloro4-iodophenyl)-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide | HCID 54268602 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | (R)-N-[2-Chloro-4-(N-phenylcarbamoyl)phenyl]-2-hydroxy-2methyl-3,3,3-trifluoropropanamide | HCID 69752005 | — |
Reaction Steps
A mixture of (R)-N-(2-chloro-4-iodophenyl)-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide (Example 197) (0.35 g), aniline (0.117 ml), tributylamine (0.232 ml) and dichlorobis-(triphenylphosphine)palladium(II) (0.009 g) was heated at 100° C. under an atmosphere of carbon monoxide for 4 hours. Ethyl acetate (10 ml) was added and the mixture was washed with water and brine then was dried. Volatile material was removed by evaporation and the residue was purified by chromatography on a silica gel Mega Bond Elut column eluting with 5-50% ethyl acetate/hexane followed by passing through a Varian Isolute SCX column to give the title compound (0.17 g) as a solid. NMR: 1.6 (s, 3H), 7.1 (t, 1H), 7.35 (t, 2H), 7.75 (d, 2H), 7.92 (s, 1H), 7.98 (dd, 1H), 8.12 (s, 1H), 8.2 (d, 1H), 9.8 (s, 1H), 10,26 (brs, 1H); MS (ESP−): 386.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960688B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-13dff6b18a1e4afdbc5a0a9d9105dd0b |
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| Source note | uspto-grants-2005_11 |
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