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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36827Generated: October 29, 2026

Toluene → HCID 57293177, compound

https://huagongshe.com/reaction/36827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant5-Hydroxymethyl-2,2,5-trimethyl-1,3-dioxaneHCID 373709—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant2-(Benzyloxy)ethyl TrifluoromethanesulfonateHCID 11129805—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57293177HCID 57293177100%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of 2,2-dimethyl-5-hydroxymethyl-5-methyl-1,3-dioxane (13.4 g, 0.084 mol) in 630 mL of anhydrous tetrahydrofuran was cooled to -20° C. under argon atmosphere. Then a 0.5M solution of potassium bis(trimethylsilyl)amide in toluene (168 mL, 0.084 mol) was added and the mixture was stirred at -20° C. for 1 hr. The 2-benzyloxyethyltriflate (23.8 g, 0.084 mol) was added neat, keeping the temperature between -20° and -15° C. The resulting solution was stirred at this temperature for 1 hr, then gradually allowed to warm to 25° C. and stirred for 15 hrs. Dichloromethane (900 mL) was added and the solution was washed twice with 300 mL of water and once with 100 mL of saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and evaporation of the solvents under reduced pressure gave 2,2-dimethyl-5-benzyloxyethoxymethyl-5-methyl-1,3-dioxane (24.6 g, 0.084 mol, 100%) which was not purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05417959
Source datasetuspto-grants-1995_05
ORD IDord-ce6759d5b59c49ff9fe8c980a9e44a64
Source noteuspto-grants-1995_05