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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTributylamineHCID 7622—
ReactantEthyl AcetateHCID 8857—
Reactant(R)-N-(2-chloro4-iodophenyl)-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 54268602—
CatalystHCID 178418476HCID 178418476—
Product(R)-N-[2-Chloro-4-(N-phenylcarbamoyl)phenyl]-2-hydroxy-2methyl-3,3,3-trifluoropropanamideHCID 69752005—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960688B2
Source datasetuspto-grants-2005_11
ORD IDord-13dff6b18a1e4afdbc5a0a9d9105dd0b
Source noteuspto-grants-2005_11