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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107803Generated: November 1, 2026

4'-Hydroxyacetophenone → HCID 13482750, compound

https://huagongshe.com/reaction/2107803

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantPotassiumHCID 5462222—
SolventDimethylformamideHCID 6228—
ProductHCID 13482750HCID 1348275090.7%

Reaction Steps

To a solution of the potassium salt of 4-hydroxyacetophenone (25.0 g, 0.14 mol) in DMF (100 ml) is added ethyl 2-chloropropanoate (27.3 g, 0.20 mol) over 30 minutes and stirred at 85°-90° C. for 3 under nitrogen. The reaction is filtered to remove KC1 and the filtrate is concentrated under reduced pressure to remove DMF and the product is analyzed by GLC. The product is dissolved ine thyl acetate (300 mL) and extracted with 2N NaOH (2x 100 mL) and water (100 mL). The organic phase is dried and concentrated to give pure ethyl 2-(4-acetylphenoxy)-propanoate (30 g) (yield 75%); m.p. 49.6° C.; IR (KBr) 1747.7 (vs), 1669.8 (vs); 1H NMR (CHCl3) delta 1.18 (t, J=7.2 Hz, 3H), 1.58 (d, J=6.8 Hz, 3H), 2.46 (s, 3H), 4.15 (q, J=7.2, 2H), 4.77 (q, J=6.8, 1H), 6.83 and 7.84 (dd, J=9.0 Hz, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935522
Source datasetuspto-grants-1990_06
ORD IDord-3c4a5ae9b0ec452b98a27e9bf9455195
Source noteuspto-grants-1990_06