HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → HCID 59011488, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57564136 | HCID 57564136 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59011488 | HCID 59011488 | — |
Reaction Steps
410 mg of tert-butyl cyclopropylsulfamoylcarbamate, 150 μl of 1,2-dibromoethane and 719 mg of K2CO3 were boiled under reflux in 6 ml of anhydrous acetone for 9 hours. The reaction mixture was left to stand at RT for 15 hours. Then 20 mg of tetrabutylammonium iodide were added, and the mixture was boiled under reflux for 9 hours. It was then diluted with 100 ml of EA and washed twice with 10 ml of water each time. After drying over Na2SO4, the solvent was removed in vacuo. 400 mg of a colorless oil were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772262B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-d719020123514cfd9694f5c2d9a16d7f |
| Source note | uspto-grants-2010_08 |