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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643934Generated: October 30, 2026

Allyl bromide → 3,6-Bis-allyloxy-5-nitrobenzo[d]isoxazole

https://huagongshe.com/reaction/643934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178526404HCID 178526404—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3,6-Bis-allyloxy-5-nitrobenzo[d]isoxazoleHCID 66750987—

Reaction Steps

To a suspension of 5-nitrobenzo[d]isoxazole-3,6-diol (1.1 g, 5.61 mmol) and potassium carbonate (3.9 g, 28.2 mmol) in DMF (10 mL) is added dropwise allyl bromide (1.42 mL, 8.30 mmol). The mixture is stirred at room temperature for 18 h. The mixture is diluted with EtOAc, and ice and water are added. The organic phase is separated and washed with water and brine, and dried over MgSO4, filtered and concentrated to afford 3,6-bis-allyloxy-5-nitrobenzo[d]isoxazole as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700633B2
Source datasetuspto-grants-2010_04
ORD IDord-2c906fd46f1a49499d32b446c10ea8d7
Source noteuspto-grants-2010_04