HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173519Generated: November 1, 2026
Formaldehyde → Resorcinol-formaldehyde resin
https://huagongshe.com/reaction/1173519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Resorcinol | HCID 5054 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Catalyst | Azane;hydrate | HCID 12896473 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Resorcinol-formaldehyde resin | HCID 159980 | 268% |
Reaction Steps
After 280 g of water and 523.6 g of resorcinol were placed in a 2 L flask made of glass and the whole dissolved at 50° C., 1.2 g of p-toluenesulfonic acid was charged into the reaction vessel. While the reaction system was maintained at 120 to 125° C., 224 g of 37% formalin was added dropwise over a period of 300 minutes and, after the completion of the dropwise addition, the mixture was further stirred for 60 minutes to cause a reaction to proceed. After the temperature of the reaction system was cooled to room temperature, 792 mL of toluene was added to a neutralized solution neutralized with 0.7 g of 25% ammonia water, followed by extraction. The extraction step was repeated twice and 524 g of water was charged. After azeotropic distillation, the residue was cooled to obtain 893 g of a resorcinol-formalin resin (content of resorcinol: about 14%, solid content: 500 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834124B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-e641c278b309464fa9c18431fc519631 |
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| Source note | uspto-grants-2010_11 |
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