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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-hydroxy-1H-pyrazoleHCID 3016733—
Reactant1-(2-Bromoethoxy)-4-(tert-butoxy)benzeneHCID 15018832—
SolventDimethylformamideHCID 6228—
Product1-[2-(4-tert-Butoxyphenoxy)ethoxy]-1H-pyrazoleHCID 1501883393%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05221684
Source datasetuspto-grants-1993_06
ORD IDord-eebd2dd53b924a1fb391c924852a6e9f
Source noteuspto-grants-1993_06