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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077336Generated: November 1, 2026

1,3-Butadiene → HCID 21292556, compound

https://huagongshe.com/reaction/1077336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-ButadieneHCID 7845—
Reactant5-Nitronaphthalene-1,4-dioneHCID 12336402—
SolventEthanolHCID 702—
ProductHCID 21292556HCID 2129255689%

Reaction Steps

24.8 g of crude 5-nitronaphthoquinone (comprised of 82 wt% of 5-nitronaphthoquinone and 10 wt% of 6-nitronaphthoquinone), 12.1 g of 1,3-butadiene, and 124 g of ethanol were introduced into an autoclave. The autoclave was hermetically sealed and the reaction was effected at about 80°C for 2.5 hours. The resultant reaction solution was cooled to 25°-30°C to crystalize 5-nitrotetrahydroanthraquinone, and filtered. The cake was washed with 40 g of ethanol and dried to obtain 22.9 g of 5-nitrotetrahydroanthraquinone. The yield was 89.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959318
Source datasetuspto-grants-1976_05
ORD IDord-5332c618108e4c3ab5370489a08169ee
Source noteuspto-grants-1976_05