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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247608Generated: October 28, 2026

Sodium hydride → HCID 14148373, compound

https://huagongshe.com/reaction/247608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,6-Di-tert-butylphenolHCID 31405—
Reactant1-Butyl-1H-pyrrole-2,5-dioneHCID 239780—
ReactantSodium t-butoxideHCID 23676156—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 14148373HCID 1414837312%

Reaction Steps

To a solution of sodium tert-butoxide prepared from 2.40 g (0.1 mol) of sodium hydride and 135 ml of tert-butyl alcohol is added dropwise a solution of 20.63 g (0.1 mol) of 2,6-di-tert-butylphenol in 100 ml of tert-butyl alcohol. The reaction mixture is stirred at room temperature for 150 minutes and then to the resultant green solution is added dropwise over 120 minutes a solution of 15.31 g (0.1 mol.) of N-n-butylmaleimide in 50 ml of tert-butyl alcohol. The reaction mixture is stirred at room temperature overnight and is then mixed with 10 ml of glacial acetic acid. The reaction mixture is poured into 1.5 1 of water and the resultant mixture is extracted twice with chloroform. The organic extracts are combined and dried over anhydrous sodium sulfate. The solvent is removed in vacuo and the residue is purified by flash chromatography (3:1 heptane:toluene eluent) to give 4.25 g (12%) of a white solid: mp 109°-112° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709050
Source datasetuspto-grants-1987_11
ORD IDord-0ba0710192d5404fb69e4eb32706a858
Source noteuspto-grants-1987_11