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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654257Generated: October 26, 2026

M-Cresol → m-Cresol-salicylaldehyde

https://huagongshe.com/reaction/654257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-CresolHCID 342—
Reactant3-Mercaptopropionic AcidHCID 6514—
Reactant2,6-Dimethylol-p-cresolHCID 7039—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventAcetic AcidHCID 176—
Productm-Cresol-salicylaldehydeHCID 86745981—

Reaction Steps

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-toluenesulfonic 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 salicyaldehyde 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, M n, of 1472 Daltons and a Tg of 233° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130410
Source datasetuspto-grants-1992_07
ORD IDord-b5d4def687124d1bbfab6d4cebf3466c
Source noteuspto-grants-1992_07