HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161671Generated: October 29, 2026
1,3-Benzodioxole → 1-Bromo-3,4-(methylenedioxy)benzene
https://huagongshe.com/reaction/1161671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Benzodioxole | HCID 9229 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Bromo-3,4-(methylenedioxy)benzene | HCID 75831 | — |
Reaction Steps
A mixture of ceric ammonium nitrate (9.88 g, 18.0 mmol) and lithium bromide (1.5 g, 18.0 mmol) in acetonitrile (20 mL) was stirred for 30 minutes at 25° C. under nitrogen atmosphere. A solution of benzo[1,3]dioxol (2 g, 16 mmol) in acetonitrile (20 mL) was added slowly to it and the mixture was stirred for 4 hours at 25° C. The mixture was then diluted with water (50 mL) and extracted with ethyl acetate (3×50 mL). The organic layers were collected, combined, washed with water (50 mL), dried over anhydrous sodium sulphate, and concentrated under vacuum to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07820654B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-1a28b934bcd84d12bac9f20b610b4af7 |
|---|
| Source note | uspto-grants-2010_10 |
|---|