Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Orcinol | HCID 10436 | — |
| Reactant | 2-Hydroxy-6-methylbenzaldehyde | HCID 585174 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86738797 | HCID 86738797 | — |
Reaction Steps
Into a reactor equipped with a thermometer, an agitator, a reflux cooler and a dropping funnel were charged 108 parts of m-cresol, 108 parts of water and 1.1 parts of potassium hydroxide, and 142 parts of 37% aqueous formaldehyde solution was added dropwise to the mixture in 2 hours while agitating the resulting mixture at 60° C. After completion of the addition of the formaldehyde solution, an agitation was further continued for 3 hours at 60° C., and then the mass was cooled to obtain a homogeneous transparent resol type precondensate of m-cresol. Into another reactor having the same equipments as described above were charged 248 parts of 5-methylresorcin, 290 parts of water and 2.5 parts of oxalic acid. Then, the above obtained m-cresol-formaldehyde reaction liquid was added dropwise to the 5-methylresorcin solution in 2 hours while agitating the resulting mixture at 60° C. After completion of the addition, the resulting mixture was further agitated at 60° C. for 3 hours, and then water in the reaction liquid was removed. The residue was poured into a distillation vessel, and unreacted m-cresol and 5-methylresorcin were removed by a distillation under reduced pressure to obtain a m-cresol/5-methylresorcin/formaldehyde cocondensate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04374962 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-2d0b14eafa044a2c934bdef7872dca5f |
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| Source note | uspto-grants-1983_02 |
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