Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578252Generated: October 26, 2026

N-methyl-2-pyrrolidone → Anthrarufin

https://huagongshe.com/reaction/1578252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant9,10-Anthracenedione, 1,2-dinitro-HCID 42596—
ReactantSodium FormateHCID 2723810—
Product1,8-DihydroxyanthraquinoneHCID 29507.5%
ProductAnthrarufinHCID 832892.5%

Reaction Steps

Dinitroanthraquinone (same composition as in Example 2, 18.0 g; 0.06 mole), N-methylpyrrolidone (100 ml) and sodium formate (12.2 g; 0.18 mole) were stirred at 110° C. for 16 hours while air was sparged into the reaction mass. Product work-up as in Example 1 gave a cake of 1.9 g (92.5% 1,5-dihydroxyanthraquinone, 7.5% 1,8-dihydroxyanthraquinone) and a filtrate product of 12.0 g (4.0% 1-hydroxyanthraquinone, 88% 1,5- and 1,8-dihydroxyanthraquinone, 2.7% intermediate and 5.3% dinitroanthraquinones).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04292248
Source datasetuspto-grants-1981_09
ORD IDord-3a77e01e32fd4f7e82853e9b8fd56492
Source noteuspto-grants-1981_09