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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714003Generated: October 25, 2026

Acetal → 1,1,3-Triethoxy-2-methyl-butane

https://huagongshe.com/reaction/714003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetalHCID 7765—
ReactantEthyl 1-propenyl etherHCID 13570—
ReactantSodium BicarbonateHCID 516892—
CatalystAluminum(III) ChlorideHCID 6451240—
Product1,1,3-Triethoxy-2-methyl-butaneHCID 1183054488%

Reaction Conditions

Temperature50 °C

Reaction Steps

236 g of acetaldehyde diethyl acetal (abbreviation: acetal) and 1 g of aluminum chloride are added in 500 ml of four necked bottle under protection of nitrogen, the solution is freezed to −10° C., and kept at −10° C.˜−5° C., a mixture of 118 g of acetaldehyde diethyl acetal and 86 g (0.945 mol) of ethyl-(1-propenyl)-ether is slowly dropped, and continue to stir it for 10 min after finishing dropping, and the end of reaction is detected by GC. A saturated NaHCO3 solution is added in the reaction to neutralize it to pH=7, and to layer, the oil layer is dried by anhydrous sodium sulfate after being washed by water, and heated to 50° C.; most of acetaldehyde diethyl acetal is recycled, to obtain 169.6 g of 1,1,3-triethoxy-2-methyl-butane by vacuum distillation, and its content is 97.2%, and its yield is 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187394B2
Source datasetuspto-grants-2015_11
ORD IDord-3ee62605852e49bfa7d087d4d683f11c
Source noteuspto-grants-2015_11