Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418808Generated: November 2, 2026

Bromine → 7-Bromo-3,4-dihydro-5,8-dimethyl-1(2H)-naphthalenone

https://huagongshe.com/reaction/1418808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1(2H)-Naphthalenone, 3,4-dihydro-5,8-dimethyl-HCID 99334—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product7-Bromo-3,4-dihydro-5,8-dimethyl-1(2H)-naphthalenoneHCID 53761320100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 15.0 g of 5,8-dimethyltetralone (purchased from Wiley Organics) in 250 mL of methylene chloride was added 28.7 g of aluminum chloride (purchased from Aldrich Chemical Co.). The mixture was cooled to 0° C. and then a solution of 15.2 g bromine in 90 mL of methylene chloride was added dropwise. After the mixture was stirred at room temperature for 2 h, it was cooled to 0° C. and then approximately 200 g of ice was added. The resulting mixture was filtered. The organic layer was separated and was washed with 1N aqueous sodium hydroxide, dried over MgSO4, filtered, and concentrated under reduced pressure. The resulting solid was crystallized from 1-chlorobutane to give 21.8 g of the title compound of Step A as a solid melting at 64°-68° C. 1H NMR (CDCl3): δ 2.11 (m, 2H), 2.25 (s, 3H), 2.64 (t, 2H), 2.66 (s, 3H), 2.77 (t, 2H), 7.53 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885936
Source datasetuspto-grants-1999_03
ORD IDord-777d173851df4b528eeb888b17c361f4
Source noteuspto-grants-1999_03