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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917662Generated: November 2, 2026

Sodium Hydroxide → 5-Benzo[1,3]dioxol-5-yl-4-bromo-oxazole

https://huagongshe.com/reaction/917662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantN-BromosuccinamideHCID 9834204—
ReactantHCID 10679193HCID 10679193—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-Benzo[1,3]dioxol-5-yl-4-bromo-oxazoleHCID 6888621590%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of 5-benzo[1,3]dioxol-5-yl-oxazole (670 mg, 3.54 mmol) in dimethylformamide (5 mL) was slowly added lithium bis(trimethylsilyl)amide(3.54 mL, 1 M in THF, 3.54 mmol, 1 equiv). The reaction mixture was stirred under nitrogen atmosphere for 1 hour at −78° C., and then treated slowly with a solution of N-bromosuccinamide (630 mg, 3.54 mmol, 1 equiv) in dimethylformamide (2 mL). The resulting reaction mixture was stirred at −78° C. for 1 hour, warmed to ambient temperature and poured into a mixture methylene chloride and 1 N aqueous sodium hydroxide. The aqueous layer was exctracted with methylene chloride, and the combined organics were washed with 1 N aqueous sodium hydroxide and brine, then dried over magnesium sulfate and concentrated in vacuo to provide 5-benzo[1,3]dioxol-5-yl-4-bromo-oxazole (853 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273936B2
Source datasetuspto-grants-2007_09
ORD IDord-7cd803ba680441adb25e2eec70f74962
Source noteuspto-grants-2007_09