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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246811Generated: November 2, 2026

3-Fluoroaniline → HCID 17982610, compound

https://huagongshe.com/reaction/2246811

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluoroanilineHCID 9742—
Reactant2,2-Dichloro-1,4-dioxaneHCID 12424325—
ProductHCID 17982610HCID 17982610—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 12.0 g (108 mmol) of 3-fluoraniline and 16 g of 2-chlorodioxene (contains 6% of 2,2-dichlorodioxane) is heated at 100° C. for 24 hours. The mixture is allowed to cool, and excess 2-chlorodioxene is removed under reduced pressure, giving 25 g of 2-(2-chloroethoxy)-N-(3-fluorophenyl)acetamide as brown oil; ESI 232. This oil is dissolved in 400 ml of acetonitrile, and 84.7 g (260 mmol) of caesium carbonate are added. The suspension formed is stirred at room temperature for 18 hours. The reaction mixture is filtered, and the filtrate is evaporated, giving 21.0 g of 4-(3-fluorophenyl)morpholin-3-one as brown oil; ESI 196. 1H-NMR (d6-DMSO): δ=3.77 (t, J=5 Hz; 2H), 3.97 (t, J=5 Hz; 2H), 4.23 (s; 2H), 7.11 (dddd, J1=8 Hz, J2=8 Hz, J3=2 Hz, J4=0.5 Hz, 1H), 7.26 (ddd, J1=8 Hz, J2=2 Hz, J3=0.5 Hz, 1H), 7.34 (ddd, J1=10 Hz, J2=2 Hz, J3=2 Hz, 1H), 7.45 (ddd, J1=8 Hz, J2=8 Hz, J3=7 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687624B2
Source datasetuspto-grants-2010_03
ORD IDord-f995fe82a4c44c87bb738429d8abb470
Source noteuspto-grants-2010_03