HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618055Generated: October 29, 2026
Acetyl chloride → 1-(6-Bromonaphthalen-2-yl)ethanone
https://huagongshe.com/reaction/618055
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Bromonaphthalene | HCID 11372 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 1-(6-Bromonaphthalen-2-yl)ethanone | HCID 12433082 | 43.6% |
Reaction Steps
To a cold (10° C.) mixture of 44.0 g (0.212 mol) of 2-bromonaphthalene and 34.0 g (0.255 mol) of aluminum chloride in 400 ml of nitrobenzene was added 21.0 g (267 mmol) of acetyl chloride. The mechanically stirred reaction mixture was warmed to room temperature, and heated to 40° C. for 18 hours. After cooling to 0° C. in an ice bath, the reaction was quenched by the addition of 12M HCl (70 ml). The layers were separated and the organic phase was washed with water and dilute aqueous Na2CO3. Kugelrohr distillation, followed by recrystallization from 10% EtOAc-hexane yielded 23 g of the title compound as a tan solid. 1H NMR (CDCl3): δ 8.44 (1H, br s), 8.04-8.10 (2H, m), 7.85 (1H, d, J=8.5 Hz), 7.82 (1H, d, J=8.8 Hz), 7.64 (1H, d, J=8.8 Hz), 2.73 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05952345 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-8697bfe66a6148f1bcfec9b7ffa6f523 |
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| Source note | uspto-grants-1999_09 |
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