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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127661Generated: October 26, 2026

Hydrochloric Acid → 5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedimethanol

https://huagongshe.com/reaction/127661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantChloroformHCID 6212—
Reactant4-tert-ButylphenolHCID 7393—
ReactantSodium HydroxideHCID 14798—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedimethanolHCID 15098199%

Reaction Conditions

Temperature60 °C

Reaction Steps

200 grams (1.331 moles) of para-t-butylphenol and 400 ml. of water were placed in a 2-liter, 3-neck, round bottom flask fitted with a thermometer, a stirrer and a dropping funnel. The flask was placed in a water bath, the contents stirred and 106.6 grams (1.331 moles) of 50% aq. NaOH added. The temperature of the resulting slurry was adjusted to 30° C. (by cooling) and 227 grams (~2.8 moles) of 37% formalin added. The mixture was heated to 60° C. and stirred at that temperature for 4 hours. It was then cooled to 35° C. and 444 ml. (1.331 moles) of 3 N aq. HCl were added. Enough dilute acetic acid was then added to make the mixture just acid. 100 ml. of chloroform was stirred in and the phases allowed to separate. The chloroform layer, containing essentially all of the product resin, was removed, washed once with water, dried by azeotropic distillation and stripped in vacuo. 276 grams (99% yield) of the title product was obtained as a resinous residue which crystallized on standing; equivalent wt. 220 grams per phenolic --OH (vs 212, theoretical).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256844
Source datasetuspto-grants-1981_03
ORD IDord-53502b33ddb74b629c44abc94f73fd7f
Source noteuspto-grants-1981_03