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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613360Generated: October 30, 2026

Ammonia → 1-(2-Hydroxyethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane

https://huagongshe.com/reaction/613360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
Reactant1-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octaneHCID 18327363—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Hydroxyethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 1832737260%

Reaction Steps

To liquid ammonia (35 ml) was added, under an argon atmosphere, a solution of 1-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane (3.54 g) in anhydrous tetrahydrofuran (8 ml). Metallic sodium (500 mg) was then added thereto, and the resultant mixture was stirred for 3 hours at -78° C. After ammonium chloride was added to the reaction mixture, ammonia was evaporated, and tetrahydrofuran was evaporated under reduced pressure. The residue was washed with ether, and the resultant solid was added to saturated brine and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, to give 1-(2-hydroxyethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane (1.4 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008224
Source datasetuspto-grants-1999_12
ORD IDord-e9c922c18aeb4c3aaed223d9a876843c
Source noteuspto-grants-1999_12