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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570754Generated: October 26, 2026

Triethylamine → HCID 86673886, compound

https://huagongshe.com/reaction/570754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluoro-3-nitrobenzoic acidHCID 18672992—
ReactantHCID 86665276HCID 86665276—
SolventDichloromethaneHCID 6344—
ProductHCID 86673886HCID 8667388643.1%

Reaction Steps

To a solution of 2-bromo-6-chloro-4-(1,2,2,3,3,3-hexafluoro-1-trifluoromethyl-propyl)phenylamine (Example I 8.1) (20 g, 47.1 mmol) and 2-fluoro-3-nitrobenzoic acid (17.4 g, 94.2 mmol) in dichloromethane (230 ml) was added triethylamine (19.7 ml, 141 mmol) and bis(2-oxo-3-oxazolidinyl)phosphonic chloride (“BOP-Cl”) (23.98 g, 94 mmol). The reaction mixture was heated to reflux for 6 hours. The reaction mixture was cooled to ambient temperature and quenched by the addition of aqueous hydrochloric acid (1N). The mixture was then extracted three times with dichloromethane. The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate, dried over sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel (eluent: cyclohexane/ethyl acetate 7:3) to give N-[2-bromo-6-chloro-4-(1,2,2,3,3,3-hexafluoro-1-trifluoromethylpropyl)phenyl]-2-fluoro-3-nitrobenzamide (12 g, 43% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023873B2
Source datasetuspto-grants-2015_05
ORD IDord-311a4a3d18d2434fbeb26fc50fb4bc4e
Source noteuspto-grants-2015_05