HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523956Generated: October 25, 2026
N-bromobutanimide → HCID 118143116, compound
https://huagongshe.com/reaction/523956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2-Difluoro-1,3-dioxaindan-4-amine | HCID 2736891 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118143116 | HCID 118143116 | 64.2% |
Reaction Steps
To a stirred solution of 4-amino-2,2-diflouro-1,3-benzodioxole (2.5 g, 14.4 mmol) in dichloromethane at 0° C. was added N-bromosuccinimide (2.7 g, 15.2 mmol) portion wise. The solution was stirred at 0° C. for 30 min, then at room temperature for 1 h. The reaction mixture was quenched with 1M sodium thiosulfate solution and diluted with deionized water, extracted with dichloromethane (2×50 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, 0-20% ethyl acetate in hexanes) to recover starting material 1 g and afford 5-bromo-4-amino-2,2-diflouro-1,3-benzodioxole as colorless oil (2.33 g, 9.25 mmol, 64%). MS: (ES) m/z calculated for C7H4BrF2NO [M+H]+252.0. found 252.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09340509B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-ca80740c073c413ca1f23ddfff5a55c5 |
|---|
| Source note | uspto-grants-2016_05 |
|---|