HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254812Generated: October 31, 2026
Potassium bis(trimethylsilyl)amide → HCID 86619474, compound
https://huagongshe.com/reaction/254812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 86619475 | HCID 86619475 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86619474 | HCID 86619474 | 91% |
Reaction Steps
To a solution of 2-tert-butyl-5-(5-(4-chlorophenyl)-4-(2,2-dibromovinyl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)-1,3,4-oxadiazole (230 mg, 0.36 mmol) in tetrahydrofuran (10 ml) at 78° C., potassium bis(trimethysilyl)amide (1.46 ml, 0.5 M solution in tetahydrofuran, 0.73 mmol) was added slowly. After stirring for 20 minutes at 78° C., the resulting solution was quenched with saturated ammonium chloride (5 ml). After warming up to room temperature, the solution was diluted with ethyl ether, and then the organic layer was extracted with ethyl acetate (50 ml twice). After evaporation, crude residue was purified with silica gel column (hexane/ethyl acetate=5/1) to obtain title compound (150 mg, 91% yield) as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875647B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-4153e5677b3541a98906c7a439d1afb6 |
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| Source note | uspto-grants-2011_01 |
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