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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743086Generated: October 26, 2026

Water → Benzene, 1-(2,2-dimethoxyethoxy)-4-(1,1-dimethylethyl)-

https://huagongshe.com/reaction/743086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-tert-ButylphenolHCID 7393—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
SolventDimethylformamideHCID 6228—
ProductBenzene, 1-(2,2-dimethoxyethoxy)-4-(1,1-dimethylethyl)-HCID 308571894.6%

Reaction Steps

To a mixture of 5.33 g (0.133 mol.) of sodium hydride (60%) and 200 ml of anhydrous N,N-dimethylformamide, there was added dropwise a solution of 20.00 g (0.133 mol.) of 4-(1,1-dimethylethyl)phenol in 50 ml of anhydrous N,N-dimethylformamide with stirring at a temperature of from 5° C. to 10° C. for 10 minutes. Then the reaction mixture was stirred at the same temperature for 30 minutes. To the above mixture, there was added dropwise 24.75 g (0.146 mol.) of bromoacetoaldehyde dimethylacetal in 50 ml of anhydrous N,N-dimethylformamide with stirring at the same temperature for 30 minutes. The reaction mixture was then stirred at room temperature for 20 hours. After the reaction was completed, the reaction mixture was poured into water and extracted with ethyl acetate. Then the residue was washed three times with a saturated aqueous solution of ammonium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography to give 30.00 g of 2-[4-(1,1-dimethylethyl)phenoxy]-1,1-dimethoxyethane as a light-yellowish oily substance (nD22.6 1.4911).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556867
Source datasetuspto-grants-1996_09
ORD IDord-041ec7520b32477187e7411c07bc685b
Source noteuspto-grants-1996_09