HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Dibenzyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Phosphorous acid | HCID 107909 | — |
| Reactant | (2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone | HCID 14863583 | — |
| Catalyst | Iridium tetrachloride | HCID 24815 | — |
| Product | Dibenzyl ether | HCID 7657 | — |
| Product | 2,3-Bis(hydroxymethyl)cyclobutanol | HCID 54083535 | — |
Reaction Steps
A mixture of (2S-trans) -2,3-bis [(benzyloxy)-methyl]cyclobutanone (0.25 g., 0.806 mmole), iridium tetrachloride (0. 016 g., 0. 0483 mmole), phosphorous acid (0.397 g., 4.84 mmole) and water (0.3 ml.) in isopropanol (3 ml.) was refluxed overnight. The solvent was evaporated on a rotary evaporator. The residue was taken up in ethyl acetate and washed successively with 10% hydrochloric acid, brine, and 5% sodium bicarbonate. The organic layer was dried (magnesium sulfate) and the solvent was evaporated to give [1α, 2β, 3β)]-3-hydroxy-1,2-cyclobutane-dimethanol, dibenzyl ether; TLC (40% ethyl acetate/hexane) Rf = 0.51.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516903 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-2198379b9c094fa9b4d9279dd5c0e475 |
| Source note | uspto-grants-1996_05 |