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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363806Generated: November 2, 2026

4-Nitrophenol → HCID 10867911, compound

https://huagongshe.com/reaction/363806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13092422HCID 13092422—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 10867911HCID 1086791171.1%

Reaction Steps

Into N,N-dimethyl formamide (200 ml) were suspended 11 g (0.27 mol) of 60%-sodium hydride. With stirring under ice cooling, an N,N-dimethyl formamide (150 ml) solution containing 38 g (0.27 mol) of p-nitrophenol was added dropwise therein over three hours. After the resulting solution was continuously stirred for further one hour as it was, the reaction liquid became a homogeneous yellow solution. The reaction liquid was returned to room temperatures, and an N,N-dimethylformamide (100 ml) solution containing 38 g (0.23 mol) of (1-chloro-2-methyl-3-butene-2-yl) acetate was added dropwise therein over three hours. The resulting mixture was stirred for additional one hour as it was. The reaction liquid was dispersed in water (1,000 ml), and 20 g of potassium carbonate were added therein, followed by stirring for one hour. After the extract obtained by extraction therefrom with ethyl acetate (500 ml) was washed with water and dried, it was concentrated under reduced pressure, thereby obtaining a yellowish brown and oily residue. This residue was purified by chromatography on a silica gel column (ethyl acetate:n-hexane system), whereby 36.5 g of the title compound were obtained. (Yield: 70.8%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874611
Source datasetuspto-grants-1999_02
ORD IDord-94ff18d0a0f54bf5972890d8bead50a0
Source noteuspto-grants-1999_02