HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579670Generated: October 26, 2026
Hydrochloric Acid → 5-Nitronaphthalene-1,4-dione
https://huagongshe.com/reaction/1579670
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178516261 | HCID 178516261 | — |
| Catalyst | Ferrous chloride tetrahydrate | HCID 16211588 | — |
| Product | 5-Nitronaphthalene-1,4-dione | HCID 12336402 | — |
Reaction Steps
42 g (0.21 mol) of iron (II) chloride tetrahydrate and 11 g (0.05 mol) of 8-nitro-1,4-naphthoquinone-1-oxime are introduced into 120 ml quantities of the solvents indicated in Table I below. While gaseous hydrogen chloride is slowly passed through them, the mixtures are left to react with continuous stirring at the temperatures indicated in Table I below until the respective reactions are complete. The increases in weight indicated in Table I below are obtained. After the reaction times specified in Table I, the mixtures are poured onto 500 ml of water heated to approximately 40°C, followed by stirring for 30 minutes. The 5-nitro-1,4-naphthoquinone formed is filtered off under suction, washed off under suction, washed with water until neutral and dried at 50°C. The yields of 5-nitro-1,4-naphthoquinone specified in Table I below in g and percent of the theoretical yield are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931255 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-ca2706cb0efb4efdbd1ad1c225711fc2 |
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| Source note | uspto-grants-1976_01 |
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