Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350733Generated: November 1, 2026

Bromine → 5-Bromo-2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazole

https://huagongshe.com/reaction/350733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazoleHCID 23061757—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-methyl-4-(5,6,7,8-tetrahydronaphthalen-2-yl)oxazoleHCID 2306194395%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183276B2
Source datasetuspto-grants-2007_02
ORD IDord-6dd76135a9c34487a0a9881deac33fff
Source noteuspto-grants-2007_02