Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | 4-Nonylphenol | HCID 1752 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Tert-octylphenol | HCID 8814 | — |
| Product | HCID 86738986 | HCID 86738986 | — |
Reaction Steps
206 g (1 mole) of p-tert-octylphenol, 220 g (1 mole) of p-nonylphenol, 100.1 g (2.67 moles) of 80% paraformaldehyde and 0.8 g of p-toluenesulfonic acid were reacted under water reflux at 100° C. for 10 hours. A reaction intermediate was obtained consuming 85% of the used formaldehyde. Phenol (94 g; 1 mole) was added to the reaction intermediate, and reacted for 3 hours. The reaction mixture was then heated to 170° C. to dehydrate it and thereby to give a pale brown p-tert-octylphenol/p-nonylphenol/phenol/formaldehyde co-condensate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04400492 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-2051905108794b1b851a9c6fb3771660 |
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| Source note | uspto-grants-1983_08 |
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