HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 5-Bromo-2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazole | HCID 23061757 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazole | HCID 23061943 | 95% |
Reaction Steps
To a solution of 2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazole (9.0 g) in dichloromethane (90 mL) was added dropwise a solution of bromine (2.2 mL) in dichloromethane (5 mL) at room temperature. After stirring the mixture at room temperature for 30 min, saturated aqueous sodium hydrogen carbonate was added, and the mixture was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate and concentrated to give 5-bromo-2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazole (11.7 g, yield 95%) as crystals. Recrystallization from ethanol gave colorless plate crystals. melting point: 97–98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183276B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-6dd76135a9c34487a0a9881deac33fff |
| Source note | uspto-grants-2007_02 |