HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172017Generated: October 25, 2026
2,5-Dihydroxyterephthalic acid → 4,6-Diamino-1,3-benzenediol 2,5-dihydroxyterepthalic acid
https://huagongshe.com/reaction/1172017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dihydroxyterephthalic acid | HCID 69131 | — |
| Reactant | 4,6-Diaminoresorcinol Dihydrochloride | HCID 2733648 | — |
| Reactant | HCID 178524618 | HCID 178524618 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4,6-Diamino-1,3-benzenediol 2,5-dihydroxyterepthalic acid | HCID 131728418 | — |
Reaction Steps
7 Parts by weight of 4,6-diamino-1,3-benzenediol dihydrochloride was dissolved in 33 parts by weight of water deaerated with nitrogen. 6.180 Parts by weight of 2,5-dihydroxyterephthalic acid was dissolved in 64 parts by weight of a 1M sodium hydroxide aqueous solution, followed by deaeration with nitrogen. The 4,6-diamino-1,3-benzenediol dihydrochloride aqueous solution was dropwise added to the 2,5-dihydroxyterephthalic acid disodium salt aqueous solution over 10 minutes to form a white precipitate of 4,6-diamino-1,3-benzenediol/2,5-dihydroxyterepthalic acid salt. In this case, the reaction temperature was maintained at 90° C. The resultant salt was recovered by filtering and dispersed in, and mixed with, 3,000 parts by weight of water deaerated with nitrogen, followed by re-filtering. Procedures of the above dispersing/mixing and filtering were repeated 3 times.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833644B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-dea1617d1fab4018b964b1ee9975a597 |
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| Source note | uspto-grants-2010_11 |
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