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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052941Generated: November 1, 2026

Water → HCID 86680884, compound

https://huagongshe.com/reaction/1052941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-1,3-dihydro-2-benzofuran-1,3-dioneHCID 639747—
ReactantHCID 86680883HCID 86680883—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 86680884HCID 8668088422%

Reaction Steps

4-hydroxyphthalic anhydride (6.70 g; 40.8 mmol), BHT (10 mg) and N-(11-bromoundecyl)-N-methyl acrylamide (13.00 g; 40.8 mmol) were dissolved in N,N-dimethylformamide (100 ml). Potassium carbonate (5.64 g; 40.8 mmol) was added. The yellow suspension was stirred at RT. Water (200 ml) was added to the reaction mixture after 20 d and the whole stirred for 1 h at RT. An oily white solid precipitated from the initially cloudy solution. The solvent was decanted off. The residue was dissolved in dilute aqueous Na2CO3 solution (5%; 100 ml). The milky/cloudy aqueous phase was washed with MtBE (5×100 ml). Diluted hydrochloric acid (2N, 100 ml) was added to the water phase (pH=1) and extraction with MtBE (8×100 ml) took place. The combined extracts were dried over Na2SO4, filtered and concentrated on the rotary evaporator. Chloroform (150 ml) was added to the residue and the whole stirred at RT. After 20 h the suspension was filtered. The filtration residue was washed with chloroform (50 ml) and discarded. The filtrate was concentrated on the rotary evaporator. The residue was dissolved in chloroform (50 ml). Acetonitrile (50 ml) was added. After 72 h storage at −18° C. the solvent was decanted off and the residue dried under a fine vacuum. 3.84 g (9.2 mmol; 22% yield) of a white solid was obtained (melting point: 95° C.), which dissolves very well e.g. in ethanol or acetone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393181B2
Source datasetuspto-grants-2016_07
ORD IDord-30371194de5d421eb0f539287acda143
Source noteuspto-grants-2016_07