Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062796Generated: October 26, 2026

Sodium hydride → HCID 178423918, compound

https://huagongshe.com/reaction/1062796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 178423917HCID 178423917—
SolventDimethylacetamideHCID 31374—
ProductHCID 178423918HCID 17842391844.3%

Reaction Steps

Sodium hydride (0.35 g, 60% suspension in mineral oil) was added in one portion to a stirred solution of 5-amino-1-(2-hydroxyethyl)-4-(4-methylphenyl)-1-H-pyrazol-3-ol(1.0 g) (Preparation 32) in anhydrous N,N-dimethylacetamide (20 ml) under a nitrogen atmosphere at room temperature. The initial effervescence observed subsided after 2-3 minutes and an orange/brown mixture resulted. After a further 7 minutes, tert-butyldimethylsilyl chloride (0.65 g) was added to the mixture in one portion and the reaction mixture was stirred at room temperature for 2 hours. Saturated aqueous ammonium chloride (50 ml) was added to the reaction mixture and the resulting aqueous medium was extracted with ethyl acetate (2×50 ml). The combined organic extracts were washed with water (40 ml), brine (40 ml) then dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was recrystallised from dichloromethane/hexane to give the title compound as a white solid (0.66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962923B2
Source datasetuspto-grants-2005_11
ORD IDord-6c7710999bae4edb8c7ce885be9afae7
Source noteuspto-grants-2005_11