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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907114Generated: November 2, 2026

Acetone → HCID 59612093, compound

https://huagongshe.com/reaction/1907114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-2-fluorobenzaldehydeHCID 2724908—
SolventWaterHCID 962—
ProductHCID 59612093HCID 5961209376%

Reaction Steps

To a mechanically stirred solution of 4-chloro-2-fluorobenzaldehyde (23.8 grams (g), 0.15 mole (mol)) in acetone (100 milliliters (mL)) at room temperature was added over 20 minutes (min) a solution of sodium hydroxide (NaOH, 6.6 g, 0.165 mol) in water (H2O, 400 mL). After stirring the reaction mixture overnight, dichloromethane (CH2Cl2, 100 mL) was added. The aqueous layer was separated and extracted with CH2Cl2 (100 mL), and the combined organic extracts were washed with brine and dried over magnesium sulfate (MgSO4). Solvent removal followed by Kugelrohr distillation gave 4-(4-chloro-2-fluorophenyl)-3-buten-2-one (1; 22.5 g, 76%) as a colorless liquid, which solidified upon standing: by 70-80° C., 0.1 mmHg (13.33 pascals (Pa)); 1H NMR (400 MHz, CDCl3) δ 7.59 (d, J=16.5 Hz, 1H), 7.50 (t, J=8.1 Hz, 1H), 7.22-7.12 (m, 2H), 6.76 (d, J=16.5 Hz, 1H), 2.39 (s, 3H); HRMS-ESI (m/z): calcd for C10H8ClFO, 198.024. found 198.025.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598086B2
Source datasetuspto-grants-2013_12
ORD IDord-99653acb62be4fa7bc5b3a51f1f9ce0e
Source noteuspto-grants-2013_12