HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33565Generated: October 28, 2026
Sodium Acetate → Acetic acid 2-(2-ethoxy-naphthalen-1-yl)-2-oxo-ethyl ester
https://huagongshe.com/reaction/33565
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Bromo-1-(2-ethoxy-naphthalen-1-yl)-ethanone | HCID 57455304 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Acetic acid 2-(2-ethoxy-naphthalen-1-yl)-2-oxo-ethyl ester | HCID 59796828 | 94% |
Reaction Steps
A mixture of 2-bromo-1-(2-ethoxy-naphthalen-1-yl)-ethanone (7.0 g), sodium acetate (2.0 g) and N,N-dimethylformamide (80 mL) was heated at 80° C. for 1.5 hours. After cooling to room temperature the N,N-dimethylformamide was removed under reduced pressure and the resulting residue was partitioned between dichloromethane (60 mL) and water (60 mL). The organic phase was washed with water (60 mL), brine (60 mL), dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to afford acetic acid 2-(2-ethoxy-naphthalen-1-yl)-2-oxo-ethyl ester (6.1 g, 94%) as dark red oil. 1H NMR (CDCl3): 1.45 (3H, t, J=7.0 Hz), 2.2 (3H, s), 4.2 (2H, q, J=7.0 Hz), 5.15 (2H, s), 7.2 (1H, d, J=9.4 Hz), 7.35 (1H, m), 7.45 (1H, m), 7.75 (1H, d, J=8.1 Hz), 7.85 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429607B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-57ef121f30984db79b7ad37dc62c324e |
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| Source note | uspto-grants-2008_09 |
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