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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Reactant | HCID 10679193 | HCID 10679193 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Benzo[1,3]dioxol-5-yl-4-bromo-oxazole | HCID 68886215 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07273936B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-7cd803ba680441adb25e2eec70f74962 |
|---|
| Source note | uspto-grants-2007_09 |
|---|