HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085330Generated: November 1, 2026
4'-Hydroxyacetophenone → HCID 13482750, compound
https://huagongshe.com/reaction/1085330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | Ethyl 2-chloropropionate | HCID 10807 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13482750 | HCID 13482750 | 90.7% |
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 hours 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 in ethyl acetate (300 mL) and extracted with 2N NaOH (2×100 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 (CDC13) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008439 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-d03f12a83b464691a64032251365e447 |
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| Source note | uspto-grants-1991_04 |
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