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HRID 37034作成日:2026年10月25日

M-Cresol → m-Cresol-salicylaldehyde

https://huagongshe.com/reaction/37034

反応式

関与物質

役割名称HCID仕込み量
反応物M-CresolHCID 342—
反応物3-Mercaptopropionic AcidHCID 6514—
反応物SalicylaldehydeHCID 6998—
反応物2,6-Dimethylol-p-cresolHCID 7039—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒Acetic AcidHCID 176—
生成物m-Cresol-salicylaldehydeHCID 86745981—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05419995
出典データセットuspto-grants-1995_05
ORD IDord-3a961eec5e2b42d9a9f3b2e594e0751d
出典メモuspto-grants-1995_05