Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853191Generated: October 30, 2026

Water → 7-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydro-naphthalene

https://huagongshe.com/reaction/853191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant6-Bromo-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-oneHCID 11831935—
ReactantHCID 178418370HCID 178418370—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product7-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydro-naphthaleneHCID 5742381265%

Reaction Steps

p-Tolyl magnesium bromide (1 M solution in diethyl ether, 4.2 mL, 4.17 mmol) was added slowly to a solution of 6-bromo-4,4-dimethyl-3,4-dihydro-2H-naphthalen-1-one (Compound 3, 350 mg, 1.39 mmol) in 10 mL of diethyl ether at 0° C. After stirring and warming to room temperature for 2 h, the mixture was quenched with water at 0° C., extracted with diethyl ether (3×5 mL), washed with brine (1×5 mL), dried (MgSO4) and concentrated at reduced pressure to give a light yellow oil. The crude oil was then dissolved in 10 mL of dichloromethane and stirred with 100 mg of para-toluenesulfonic acid at room temperature for 2 h. Water (10 mL) was then added and the organic layer was washed with brine (1×5 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chromatography (hexane) gave the title compound (295 mg, 65% yield) as a colorless oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253319B2
Source datasetuspto-grants-2007_08
ORD IDord-5f42998240e3467198660a9f49505fa5
Source noteuspto-grants-2007_08