HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 3-Benzyloxy-4-bromomethylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Benzyloxy-4-hydroxymethylbenzonitrile | HCID 22476097 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Benzyloxy-4-bromomethylbenzonitrile | HCID 22476099 | — |
Reaction Steps
4.3 g (18 mmol) of the alcohol (a) underwent substitution in 40 ml of THF with 7.9 g (24 mmol) of CBr4 and 6.3 g (24 mmol) of PPh3, which was added in portions over the course of 30 min. The reaction mixture was stirred at RT for 20 h. The product was purified by column chromatography (mobile phase: t-butyl methyl ether/petroleum ether 2:1). 4.6 g were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900319B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-2c0be20f28d84e488a3ed5e540001a71 |
| Source note | uspto-grants-2005_05 |