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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876375Generated: October 29, 2026

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

https://huagongshe.com/reaction/876375

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-butanesulfonyl fluoride (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% yield) as a yellow semisolid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987255B2
Source datasetuspto-grants-2015_03
ORD IDord-58ba0cfb4d7a49438f29a8ede9b4c0ff
Source noteuspto-grants-2015_03