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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361985Generated: October 28, 2026

Formaldehyde → HCID 23499685, compound

https://huagongshe.com/reaction/361985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12407526HCID 12407526—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
ProductHCID 23499685HCID 2349968582.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

Into a 100 ml four-necked flask were charged 29.96 g of 1,4-bis[1-(4-hydroxy-3-methylphenyl)-1-methylethyl]benzene["Bis-OC-P" manufactured by Honshu Kagaku Co., Ltd.], 4.48 g of sodium hydroxide and 44.8 g of water. While stirring at 50° C., 25.97 g of 37% formaldehyde was added dropwise thereto over 1 hour, and the reaction was conducted for 1 more hour. After completion of the reaction, 11 g of 90% aqueous acetic acid solution was added for neutralization and then the mixture was cooled to 25° C. Thereafter, 100 g of ethyl acetate and20 g of toluene were added thereto and a phase separation was carried out. The separated solution was concentrated and 100 g of hexane was added to the concentrated mass and it was cooled to 25° C. The resulting mixture was filtered, and the filtered product was rinsed with 100 g of hexane and dried a whole day and night at 45° C. under reduced pressure to obtain 28.75 g of 1,4-bis[1-(4-hydroxy-3-hydroxymethyl-5-methylphenyl)-1-methylethyl]benzene

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866724
Source datasetuspto-grants-1999_02
ORD IDord-6dbd6a360d6147258a07847131cac87d
Source noteuspto-grants-1999_02