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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889643Generated: October 28, 2026

Acetone → HCID 59612093, compound

https://huagongshe.com/reaction/889643

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 numberUS08252938B2
Source datasetuspto-grants-2012_08
ORD IDord-20cdbf3b64c74a0f88fdadd8b4770521
Source noteuspto-grants-2012_08