HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266678Generated: November 2, 2026
Naphthalene → 2-Methyl-1-(1-naphthalenyl)-1-propanone
https://huagongshe.com/reaction/1266678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methyl-1-(1-naphthalenyl)-1-propanone | HCID 12294683 | — |
Reaction Steps
Aluminium chloride (28.0 g, 0.21 mole) was suspended in 200 ml of anhydrous dichloromethane and was cooled to −30° C. A solution of naphthalene (25.6 g, 0.2 mole) and isobutyryl chloride (21.3 g, 0.20 mole) in 50 ml of anhydrous dichloromethane was slowly added to this suspension. After the addition was completed, the reaction mixture was stirred at −30° C. for 1 h. The reaction mixture was then allowed to warm up to room temperature. The reaction mixture was poured onto 300 g of ice water, and the organic layer was separated. The organic layer was successively washed twice with a 5 wt % aqueous hydrochloric acid solution (150 ml) and once with a 2 wt % aqueous sodium bicarbonate solution (150 ml). After drying over anhydrous magnesium sulfate the solution was concentrated under reduced pressure. The yield of 2-methyl-1-(1-naphthalenyl)-1-propanone was 39.7 g or 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548710B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-e153ca799fca48c9a5f88c195b823fc6 |
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| Source note | uspto-grants-2003_04 |
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