HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429604Erstellt: 24. Oktober 2026
Phenol → Phenol, 4,4'-[1,3-phenylenebis(1-methylethylidene)]bis-
https://huagongshe.com/de/reaction/429604
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | 1,3-Diisopropenylbenzene | HCID 77353 | — |
| Lösungsmittel | P-Xylene | HCID 7809 | — |
| Produkt | Phenol, 4,4'-[1,3-phenylenebis(1-methylethylidene)]bis- | HCID 3292100 | 15,3% |
Reaktionsschritte
A 500-ml three-neck reactor was charged with Amberlist-15 (7.5 g, 2.6 mmols), phenol (178.5 g, 633 mmols) and p-xylene (60 ml). The contents were heated up to 80° C. in nitrogen atmosphere. Under agitation, a mixture of m-diisopropenylbenzene (m-DIPeB, 15.0 g, 31.5 mmols) and p-xylene (60 ml) was fed thereto over 3 hours at 80° C. After completion of the feed, agitation was carried out at 80° C. for 10 minutes and then Amberlist-15 was removed by filtration. The filtrate was analyzed by liquid chromatography. Bisphenol M (α, α″-bis(4-hydroxyphenyl)-1,3-diisopropylbenzene, 30.5 g, yield 93%), the intended product, and the o, p-product, the position isomer of bisphenol M (α-(4-hydroxyphenyl)-α″-(2-hydroxyphenyl)-1,3-diisopropylbenzene, 1.67 g, yield 5.1%), were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06316677B1 |
|---|
| Quelldatensatz | uspto-grants-2001_11 |
|---|
| ORD ID | ord-cd31a59c7312461799936d564233f49e |
|---|
| Quellennotiz | uspto-grants-2001_11 |
|---|