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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898836Generated: October 31, 2026

Tert-Butylamine → HCID 86616350, compound

https://huagongshe.com/reaction/898836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantAcetic AnhydrideHCID 7918—
ReactantSulfur trioxideHCID 24682—
Reactant1,4-DioxaneHCID 31275—
SolventTolueneHCID 1140—
ProductHCID 86616350HCID 8661635062.5%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

The reaction time for cleavage of 1,4-dioxane was 2 hours at 120-125° C. and for animation with t-butyl amine was 30 minutes at 140-145° C. A 50 mL one-necked flask was charged with 1,4-dioxane (12 mL, 12.4 g, 140 mmol) under a nitrogen atmosphere. Then sulfur trioxide (2.6 g, 32.5 mmol, polymer) was added followed by addition of acetic anhydride (6.2 mL, 6.6 g, 65 mmol) at 10-15° C. The reaction mixture was stirred at 20-25° C. for 15 minutes to dissolve sulfur trioxide (time may very depending on size of pieces of SO3). The reaction mixture was then transferred to a sealed tube and heated at 120-125° C. for 2 hours. After cooling, the mixture was transferred to one neck 100 mL flask and concentrated under vacuum (1 mm) at 60-65° C. 1,4-dioxane (5 mL, 5.2 g, 58.7 mmol) and tert-butylamine (20 mL, 14 g, 190 mmol) were added to the residue with stirring and cooling. The mixture was transferred to a sealed tube and heated at 140-145° C. for 30 minutes. Then the reaction mixture was cooled to room temperature. Toluene (40 mL) was added with stirring and the mixture was filtered under vacuum. The precipitate was washed with toluene (10 mL) and then concentrated under vacuum to 25-30 mL. The toluene layer was separated from the insoluble bottom oil and the solvent was removed under vacuum to give crude product 2-(2-tert-butylaminoethoxy)ethyl acetate (3.8 g, 20 mmol, approximately 62.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351865B2
Source datasetuspto-grants-2008_04
ORD IDord-5b71e81bdd204a82a4dd1b770c1d7497
Source noteuspto-grants-2008_04