HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25881Generated: November 1, 2026
Hydrochloric Acid → HCID 70605606, compound
https://huagongshe.com/reaction/25881
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3,5-Triazine, 2-chloro-4,6-bis(dodecyloxy)- | HCID 590644 | — |
| Reactant | [1,1':3',1''-Terphenyl]-2',5'-diol | HCID 10563427 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70605606 | HCID 70605606 | — |
Reaction Steps
In a 500 ml-three-necked flask 4.8 g (0.01 mole) of the 2-chloro-4,6-dilauroxy-s-triazine prepared above, were mixed with 2.6 g (0.01 mole) of 2,6-diphenyl hydroquinone. After rinsing with nitrogen, 150 ml of acetone were added, followed by adding dropwise, with vigorous stilling, 0.4 g (0.01 mole) of NaOH dissolved in 7 ml of water, at 20° C. The solution then assumed an orange-yellow color, which largely disappeared upon heating the reaction mixture for a longth of time under reflux. After completion of the reaction, the contents of the flask were poured into 100 ml of ice water containing 2 ml of hydrochloric acid. The organic layer was extracted three times with methylene chloride, after which the combined extracts were washed and dried. After concentration of the organic layer by evaporation a product was obtained which crystallized out after a length of time (melting point 18°-20° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04147659 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-3f5c1017e42d4c01a4553abe59481e5b |
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| Source note | uspto-grants-1979_04 |
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