HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894864Generated: October 31, 2026
Hydrochloric Acid → 2,6-Dihydroxybenzaldehyde
https://huagongshe.com/reaction/1894864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Resorcinol | HCID 5054 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,6-Dihydroxybenzaldehyde | HCID 10285801 | — |
Reaction Steps
Mesoporous carbons with highly ordered structure were prepared using weight ratios of 1.1 resorcinol:1.1 F127:0.48 formaldehyde:3.55-8.2 ethanol:5.1-1.67 water:0.16-0.66 HCl. In a typical synthesis, 1.1 g of resorcinol and 1.1 g of F127 were dissolved in 4.5 ml of ethanol (EtOH), and to this was added 4.5 ml of 3.0M HCl aqueous solution and 1.3 g of 37% formaldehyde (37%) was then added. After stirring for 12-13 min. at room temperature, the clear mixture turned turbid, indicating the formation of the ordered nanocomposite and a phase separation. After stirring for a total of 40 minutes, the mixture was centrifuged at 9500 rpm for 4 minutes in order to completely separate and isolate the polymer-rich gel phase. The gel was then loaded on a large Petri dish and cured at 80° C. and subsequently 150° C. for 24 hours each. Carbonization was carried out under nitrogen atmosphere at 400° C. for 2 hours at a heating rate of 1° C./min followed by further treatment at 850° C. for 3 hours at a heating rate of 5° C./min. The produced carbon material is referred to as C-ORNL-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513319B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-7f959c1affc14f46814ce09eb50dace2 |
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| Source note | uspto-grants-2013_08 |
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