HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Benzyl 2-benzyloxymethyl-4-bromobutyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Benzyloxy-3-benzyloxymethylbutanol | HCID 562218 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 2-benzyloxymethyl-4-bromobutyl ether | HCID 15928659 | — |
Reaction Steps
A solution of 4-benzyloxy-3-benzyloxymethylbutan-1-ol (41.75 g, 139 mmol) in 150 ml of dry dichloromethane was cooled in ice-water bath. Triphenylphosphine (42.0 g, 160 mmol) was added with stirring and then N-bromosuccinimide (26.0 g, 146 mmol) in portions during 15 min. After 1 h at room temperature ether (400 ml) was added and the precipitated triphenylphosphine oxide filtered off. The solution was concentrated in vacuum to a small volume, and more ether was added to extract the product from precipitated triphenylphosphine oxide. Finally, this extraction-precipitation step was repeated with light petroleum to give, after evaporation, 33.55 g (66%) of crude title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04798833 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-927cc73f510d4a329ef490f0e3ea5e9f |
| Source note | uspto-grants-1989_01 |