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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 787Generated: October 24, 2026

M-Cresol → 2-Hydroxy-6-methylbenzaldehyde

https://huagongshe.com/en/reaction/787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-CresolHCID 342—
ReactantFormaldehydeHCID 712—
Reactant2,6-Dimethylol-p-cresolHCID 7039—
ReactantGlycol monoethyl ether acetateHCID 8095—
ReactantOxalic acid dihydrateHCID 61373—
SolventWaterHCID 962—
Product2-Hydroxy-6-methylbenzaldehydeHCID 585174—

Reaction Conditions

Temperature70 °C

Reaction Steps

A phenolic resin rich in alternating phenolic copolymer block segments was formed by reacting a mixture of 519.0 g of 99 percent pure m-cresol, 538.2 g of 97 percent pure 2,6-bis(hydroxymethyl)-p-cresol and 20 g oxalic acid dihydrate in a solvent mixture of 40 ml deionized water and 200 ml ethyl cellosolve acetate. The reaction mixture was heated to about 70° C. to initiate the reaction forming the alternating copolymer. At 102° C., 32.6 g of 36.9 percent formaldehyde was added in 8 minutes to the reaction mixture to form substantially m-cresol formaldehyde block segments and to chemically bond these segments to the previously formed alternating copolymer. After heating the mixture at reflux for three hours, the amount of heat was increased to remove the water and solvent by distillation. Partial vacuum was applied at about 220° C. and gradually increased to 4 mm Hg to remove the unreacted monomers. Maximum mixture temperature during vacuum stripping was about 226° C. The copolymer was poured from the reaction kettle and allowed to cool. About 840 g of a block copolymer having a number average molecular weight number, Mn, of 1241 Daltons and a Tg of 112° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723254
Source datasetuspto-grants-1998_03
ORD IDord-ddf67391f0ff4ca08b0e3124c9c5cf53
Source noteuspto-grants-1998_03