HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butylphenol → HCID 53805699, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butylphenol | HCID 18515 | — |
| Reactant | 1,8-Dibromooctane | HCID 78310 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53805699 | HCID 53805699 | — |
Reaction Steps
Two molar equivalents of the potassium salt of butylphenol and one molar equivalent of 1,8-dibromooctane are reacted in ethanol according to the procedure described in Example 1, to afford 1,8-bis (butylphenoxy) octane. Sulfonation with sulfur trioxide or chlorosulfonic acid, followed by neutralization of the disulfonic acid with methanolic potassium hydroxide, affords the potassium sulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307078 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-8625d50671c144ea9a2d599aeab01232 |
| Source note | uspto-grants-1981_12 |