HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501405Generated: October 29, 2026
Hexachloroethane → HCID 57472626, compound
https://huagongshe.com/reaction/501405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 57472624 | HCID 57472624 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57472626 | HCID 57472626 | 93.8% |
Reaction Steps
220 ml of lithium hexamethyldisilazide (1.0 M tetrahydrofuran solution) was added to a 4-L tetrahydrofuran solution of 68.3 g of 5-methyl-1-trityl-1,5-dihydroimidazo[4,5-d]pyridazin-4-one at −75° C. under a nitrogen atmosphere, and the mixture was stirred at −75° C. for 1 hour. Then, 200 ml of a tetrahydrofuran solution of 82.3 g of hexachloroethane was added to the solution. The mixture was allowed to warm to −20° C. 5 L of 5% aqueous ammonium chloride was added, and the mixture was extracted with 4 L of ethyl acetate. The organic layer was washed successively with 5 L of water and 5 L of a saturated sodium chloride solution. The solution was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was suspended in 150 ml of t-butyl methyl ether, and then collected by filtration. The solid was washed twice with 100 ml of t-butyl methyl ether to give 69.7 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07772226B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-ece8b764c29e4d65971347a3b9c430f8 |
|---|
| Source note | uspto-grants-2010_08 |
|---|