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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179864Generated: October 30, 2026

N-methyl-2-pyrrolidone → HCID 86701360, compound

https://huagongshe.com/reaction/2179864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 86701359HCID 86701359—
SolventWaterHCID 962—
ProductHCID 86701360HCID 8670136092.8%

Reaction Conditions

Temperature175 °C

Reaction Steps

Under the nitrogen atmosphere, 9-(4-ethoxynaphthalen-1-yl)anthracene (87.1 g) as the fourteenth intermediate compound, pyridine hydrochloride (289.0 g) and 1-methyl-2-pyrrolidone (87 ml) were added to a flask, and stirred for 16 hours at 175° C. The reaction solution was cooled to room temperature, added with water, and washed while being heated. After suction filtration, the solid remained after dissolution was collected. The obtained solid was washed with methanol while being heated. It was then dissolved in heated chlorobenzene and subjected to suction filtration by using a Kiriyama funnel layered with silica gel. An appropriate amount of filtrate was distilled off under reduced pressure, and by adding heptane, re-precipitation was performed to give 4-(anthracen-9-yl)naphthalen-1-ol (74.3 g) as a fifteenth intermediate compound. The scheme is shown in the following “Reaction 26”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09070885B2
Source datasetuspto-grants-2015_06
ORD IDord-553f0e7bf34341dbb3b5a0e5e0fdda11
Source noteuspto-grants-2015_06