HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33560Generated: October 29, 2026
Phenyltrimethylammonium bromide dibromide → 2-Bromo-3-methyl-1-naphthalen-1-ylbutan-1-one
https://huagongshe.com/reaction/33560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Reactant | 3-Methyl-1-naphthalen-1-ylbutan-1-one | HCID 20752065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-3-methyl-1-naphthalen-1-ylbutan-1-one | HCID 57455310 | — |
Reaction Steps
To a solution of 3-methyl-1-(naphth-1-yl)butan-1-one (20 g) in anhydrous tetrahydrofuran (150 ml) was added phenyltrimethylammonium tribromide (35.7 g). The resulting mixture was stirred overnight at ambient temperature then partitioned between petroleum ether and water. The organic layer was separated, washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo to yield crude 2-bromo-3-methyl-1-(naphth-1-yl)butan-1-one. Sodium acetate (7.7 g) and anhydrous dimethylformamide (40 ml) were added and the resulting mixture was stirred at 100° C. for 6 hours. After cooling, the mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted once with ethyl acetate. The combined organic layers were washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo. The title compound (8.4 g) was obtained following silica gel column chromatography of the residue in 50% dichloromethane in petroleum ether.
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-7a6ed1402ced4e2b88843160080d901a |
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| Source note | uspto-grants-2008_09 |
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