HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 77374747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 71349956 | HCID 71349956 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 77374747 | HCID 77374747 | — |
Reaction Steps
A solution of 6.9 g of the alcohol 3, 1.68 g of sodium hydride, 300 mg of tetrabutylammonium iodide and 5.95 g of benzyl bromide in 250 ml of THF was stirred for 4 hours at 60° C. At the end of this time 100 ml of saturated aqueous ammonium chloride solution was added and the mixture extracted with 200 ml of EtOAc and the organic phase was dried with sodium sulfate. Concentration under vacuum provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05011943 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-7897477544db4426bf061ef729688ac2 |
| Source note | uspto-grants-1991_04 |