HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Furan, tetrahydro-3-(phenylmethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 3-Furanol, tetrahydro- | HCID 9960 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Furan, tetrahydro-3-(phenylmethoxy)- | HCID 11240801 | — |
Reaction Steps
Thus, benzylchloride or benzylbromide can be reacted at elevated temperature with the alkololate from 3-hydroxytetrahydrofurane and sodium hydride, suspended in dioxane to yield the (3-tetrahydrofuryl)-benzylether which is an active herbicide against grassy weeds (German Offenlegungsschrift No. 2724675).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04331821 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-c3ed228d32a342318500e97ec64e40db |
| Source note | uspto-grants-1982_05 |