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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36834Generated: October 27, 2026

tert-Butanol → 4-(t-Butoxycarbonyl)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane

https://huagongshe.com/reaction/36834

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-Carboxy-1-methyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 19936249—
SolventAcetonitrileHCID 6342—
Product4-(t-Butoxycarbonyl)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 19936241—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 4-carboxy-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane (9.3 g, 0.053 mol) and 1,3-dicyclohexylcarbodiimide (10.9 g, 0,053 mol) in 100 mL of acetonitrile is stirred at 25° C. for 30 min. Then 2-methyl-2-propanol (3.9 g, 5.0 mL, 0.053 mol) is added and the resulting mixture is stirred for 15 hrs. The solids are filtered and the filtrate is evaporated under reduced pressure to yield 4-(t-butoxycarbonyl)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane as a crude oil. This material is dissolved in 100 mL of tetrahydrofuran and stirred with 50 mL of 10% hydrochloric acid for 1 hr. The pH of the solution is adjusted to 7 with solid sodium bicarbonate and the solvents are removed under reduced pressure. The solids are triturated with methanol and the combined methanol solutions are evaporated to give t-butyl-tris(hydroxymethyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05417959
Source datasetuspto-grants-1995_05
ORD IDord-9228ac441d88488d9fc19118be4dbdd4
Source noteuspto-grants-1995_05