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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37034Erstellt: 23. Oktober 2026

M-Cresol → m-Cresol-salicylaldehyde

https://huagongshe.com/de/reaction/37034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktM-CresolHCID 342—
Edukt3-Mercaptopropionic AcidHCID 6514—
EduktSalicylaldehydeHCID 6998—
Edukt2,6-Dimethylol-p-cresolHCID 7039—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelAcetic AcidHCID 176—
Produktm-Cresol-salicylaldehydeHCID 86745981—

Reaktionsschritte

A mixture of 146.0 g m-cresol, 25.2 g 2,6-bis(hydroxymethyl)-p-cresol, 5.0 g 3-mercaptopropionic acid and 1.5 g p-toluene-sulfonic acid monohydrate in 200 ml glacial acetic acid were charged into a 1-L reaction vessel equipped with a paddle stirrer, reflux condenser and a nitrogen inlet tube. The mixture was heated to reflux and maintained at reflux to allow formation of the alternating copolymer. After 8 hours, 146.5 g salicylaldehyde were added over time to the reaction mixture to form substantially m-cresol-salicylaldehyde block segments. Reflux was continued for 8 hours. The reaction mixture was slowly poured into 7 L deionized water to precipitate the resin. Once the solvent had exchanged with water, the product was collected on a filter, slurried once in warm deionized water for about 30 minutes, again collected, rinsed with water and dried in a vacuum oven under about 125 mm Hg and at about 100 to 105° C. About 281 g of a block copolymer resin having a number average molecular weight, Mn, of 1472 Daltons and a Tg of 233° C. were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05419995
Quelldatensatzuspto-grants-1995_05
ORD IDord-3a961eec5e2b42d9a9f3b2e594e0751d
Quellennotizuspto-grants-1995_05