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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant3-Methyl-1-naphthalen-1-ylbutan-1-oneHCID 20752065—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-3-methyl-1-naphthalen-1-ylbutan-1-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429607B2
Source datasetuspto-grants-2008_09
ORD IDord-7a6ed1402ced4e2b88843160080d901a
Source noteuspto-grants-2008_09