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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 6-Bromo-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 11831935 | — |
| Reactant | HCID 178418370 | HCID 178418370 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydro-naphthalene | HCID 57423812 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07253319B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-5f42998240e3467198660a9f49505fa5 |
|---|
| Source note | uspto-grants-2007_08 |
|---|