HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609378Generated: October 30, 2026
Hydrochloric Acid → 1,3-Benzenediol, 2-chloro-4,6-dinitro-
https://huagongshe.com/reaction/1609378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dichloro-4,6-dinitrophenol | HCID 10857978 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1,3-Benzenediol, 2-chloro-4,6-dinitro- | HCID 11107290 | 95% |
Reaction Steps
A solution of 2,3-dichloro-4,6-dinitrophenol (2.2 g, 0,008 mol, from previous example), 4.5 g of potassium t-butoxide, 0.4 g of potassium hydroxide, 30 mL of N-methyl pyrrolidinone, and 15 mL of water in a 100 mL round-bottomed flask with stir bar is heated to 85° C. for 6 hours. Upon completion, the reaction mixture is poured into 50 mL of aqueous hydrochloric acid. The resulting product is isolated by filtration, washed with cold water, and air dried. The product is recrystallized from a minimal amount of methanol to yield 1.97 g of 2-chloro-4,6-dinitroresorcinol (95% yield) (85% overall from 1,2-dichloro-3,5-dinitrobenzene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05399768 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-5b3d6a07582e4fee91bc8002b06e4fc7 |
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| Source note | uspto-grants-1995_03 |
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