HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751862Generated: October 28, 2026
Ethyl Acetate → 2-tert-butyl-4-chloro-5-(2-tert-butyldimethylsilyloxy-1-(4-tert-butylphenyl)-1-ethyl)oxy-3(2H)-pyridazinone
https://huagongshe.com/reaction/1751862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Tert-butyl-4,5-dichloro-2,3-dihydropyridazin-3-one | HCID 2782225 | — |
| Reactant | 1-Tert-butyldimethylsilyloxy-2-hydroxy-2-(4-tert-butylphenyl)ethane | HCID 59678651 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-tert-butyl-4-chloro-5-(2-tert-butyldimethylsilyloxy-1-(4-tert-butylphenyl)-1-ethyl)oxy-3(2H)-pyridazinone | HCID 67100709 | — |
Reaction Steps
To a solution of 2-tert-butyl-4,5-dichloro-3(2H)-pyridazinone (0.5 g, 2.27 mmol) in DMF (10 ml) were added anhydrous cesium carbonate (0.74 g, 2.27 mmol) and 1-tert-butyldimethylsilyloxy 2-hydroxy 2-(4-tertbutylphenyl)ethane (0.7 g, 2.27 mmol). The mixture is stirred for 2 hours at 70° C. and then cooled to room temperature and ethyl acetate is added to it. The solution is then washed with water, dried and concentrated and the residue subjected to purification by flash chromatography (silica gel; ethyl acetate/hexanes) to give the above compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09161997B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-b279612b0f5b44f480a7b4d0f5bef578 |
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| Source note | uspto-grants-2015_10 |
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