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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417679Generated: November 2, 2026

Acetyl chloride → 1-(6-Bromonaphthalen-2-yl)ethanone

https://huagongshe.com/reaction/1417679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-BromonaphthaleneHCID 11372—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitrobenzeneHCID 7416—
Product1-(6-Bromonaphthalen-2-yl)ethanoneHCID 1243308243.6%

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). 6-bromo-2-naphthalenecarboxylic acid (Compound M)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877207
Source datasetuspto-grants-1999_03
ORD IDord-b70c216b36b9407a9a507663282004ee
Source noteuspto-grants-1999_03