HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-Butylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Furfuryl Alcohol | HCID 7361 | — |
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Butylphenol | HCID 18515 | — |
Reaction Steps
1 200 Parts of p-tert-butylphenol, 800 parts of xylene, 240 parts of sodium hydroxide solution and 1 296 parts of 37% aqueous formaldehyde are reacted as in Example 1 in the apparatus of Example 1 until the formaldehyde content is 1.7%. Then, as in Example 1, the pH is adjusted to 5.5 with 25% sulphuric acid, followed by working up. 1 568 Parts of furfuryl alcohol are then added and 450 ml of aqueous phase is azeotropically distilled off at maximum temperature of 177° C. as in Example 1. After distilling off the entrainer at 130° C./100 mbar, 1 225 parts of furfuryl alcohol are added and 3 890 parts of a furan resin solution are obtained having a residue of 60% (1 hour/170° C.) and a viscosity of 4 750 mPa.s/20° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04302380 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-ed92a3bff2ac4ef2add2fcd1845c0fbb |
| Source note | uspto-grants-1981_11 |