HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36093Generated: October 26, 2026
(2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone → Dibenzyl ether
https://huagongshe.com/reaction/36093
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone | HCID 14863583 | — |
| Reactant | Triisobutylaluminum | HCID 16682931 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Dibenzyl ether | HCID 7657 | — |
Reaction Steps
A solution of (2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone (0.2 g., 0.645 mmole) in toluene (4 ml.) was added dropwise over 10 minutes to a solution of triisobutylaluminum (0.91 M in hexane, 0.9 ml., 0.816 mmole) in toluene (2 ml.) at -40° C. The mixture was stirred at -50° C. for 4 hours and at -40° C. for one hour. A solution of triisobutylaluminum (1 ml., 0.91 mmole) was added to the reaction mixture. After stirring for 30 minutes the reaction was quenched by adding 10% hydrochloric acid (2 ml.) at -40° C. The organic phase was washed with brine, dried (magnesium sulfate), and the solvent was evaporated to give [1S-(1α,2β,3β)]-3-hydroxy-1,2-cyclobutanedimethanol, dibenzyl ether; TLC (30% ethyl acetate/hexane) Rf =0.3. The product contained about 5% of the isomeric compound; TLC (30% ethyl acetate/hexane) Rf =0.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05412134 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-4dfa1debe66d46a791cd9e5f90acd2c9 |
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| Source note | uspto-grants-1995_05 |
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