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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405710Generated: October 30, 2026

Triethylamine → 2-Fluoro-1-(2-fluoro-phenyl)-ethanone

https://huagongshe.com/reaction/405710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21837678HCID 21837678—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-1-(2-fluoro-phenyl)-ethanoneHCID 2196449161%

Reaction Steps

A solution of 1-(2-fluorophenyl)-2-hydroxyethanone [CAS 218771-68-7; WO9857925, ex. 16) (2.77 g, 18.0 mmol) in dichloromethane (42 ml) was treated consecutively at 0° C. with triethylamine (6.36 g, 62.8 mmol), triethylamine trihydrofluoride (3.05 g, 18.0 mmol) and nonafluoro-n-butansulfonylfluoride (8.48 g, 26.9 mmol). The tube was sealed and the reaction mixture stirred overnight at room temperature. For the workup, the dark red solution was poured on a saturated solution of sodium hydrogencarbonate and ice, then extracted with dichloromethane. The organic layer was separated, dried over sodium sulphate and evaporated. The crude material was purified by flash chromatography on silica gel (Telos Flash Silica) using dichloromethane as the eluent to give the 2-fluoro-1-(2-fluoro-phenyl)-ethanone (1.23 g, 61% of theory) as a yellow semisolid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754075B2
Source datasetuspto-grants-2014_06
ORD IDord-519f76ae48314aca99c27b8ae1c7e844
Source noteuspto-grants-2014_06