HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588299Generated: November 3, 2026
Sodium hydride → 1-[2-(4-tert-Butoxyphenoxy)ethoxy]-1H-pyrazole
https://huagongshe.com/reaction/1588299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-hydroxy-1H-pyrazole | HCID 3016733 | — |
| Reactant | 1-(2-Bromoethoxy)-4-(tert-butoxy)benzene | HCID 15018832 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[2-(4-tert-Butoxyphenoxy)ethoxy]-1H-pyrazole | HCID 15018833 | 93% |
Reaction Steps
A solution of 12.7 g (0.15 mol) of N-hydroxypyrazole in 20 ml of DMF was added dropwise to a suspension of 4.95 g (1.1 eq.) of NaH (80% dispersion in mineral oil) in 40 ml of DMF at RT, and the mixture was heated at 70° C. for 1 h. A solution of 40.95 g (0.15 mol) of 2-[4-(1,1-dimethylethoxy)phenoxy]ethyl bromide in 100 ml of DMF was added and the mixture was then heated at 125° C. for 15 h. The solvent was then stripped off in a rotary evaporator, the residue was taken up in ethyl acetate, and the solution was washed twice each with 5% strength NaOH solution and water. Drying and removal of the solvent under reduced pressured resulted in 38.4 g (93%) of the required compound as a pale oil which was employed without further purification in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05221684 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-eebd2dd53b924a1fb391c924852a6e9f |
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| Source note | uspto-grants-1993_06 |
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