HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-[(Allyloxy)methyl]-3-ethyloxetane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Ethyl-3-hydroxy-methyloxetane | HCID 22138127 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | 3-[(Allyloxy)methyl]-3-ethyloxetane | HCID 15250358 | — |
Reaction Steps
In a flask equipped with a stirrer were placed a solution of 23.2 g (0.2 mole) of 3-ethyl-3-hydroxy-methyloxetane dissolved in 48.4 g (0.4 mole) of allyl bromide and 50 g of an aqueous solution containing 50% by weight of potassium hydroxide. Thereto was added 1.0 g of tetra-n-butylammonium bromide at 0° C. with vigorous stirring. After 24 hours, 100 ml of dichloromethane and 100 ml of water were added. The resulting organic phase was washed with water twice, dried over magnesium sulfate, and filtered. The filtrate was treated by the use of a rotary evaporator to remove the solvent in the filtrate. The residue was purified by vacuum distillation to obtain 28.6 g of 3-ethyl-3-allyloxymethyloxetane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721020 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-de4ce9aa2dca4b5ba70dda9557e73724 |
| Source note | uspto-grants-1998_02 |