HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613359Generated: October 29, 2026
Diethyl Ether → 1-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane
https://huagongshe.com/reaction/613359
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methyl-3-oxetanylmethyl 3-benzyloxypropionate | HCID 54178956 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane | HCID 18327363 | 73.9% |
Reaction Steps
3-Methyl-3-oxetanylmethyl 3-benzyloxypropionate (521 mg) was dissolved in dichloromethane under an argon atmosphere, and trifluoroborane-diethylether was added thereto at -15° C. The mixture was stirred for 5 hours at -15° C. Triethylamine (280 μl) was added to the reaction mixture, and stirring was continued for 15 minutes. Subsequently, diethylether (3 ml) was added. The precipitating crystals were removed from the reaction mixture by filtration, then the mother liquid was concentrated under reduced pressure. The residue was purified by alumina column chromatography (ethyl acetatehexane 1:3), to give 385 mg of 1-(2-benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008224 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-88d1c4cc2a814a518e7b8545e9783259 |
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| Source note | uspto-grants-1999_12 |
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