HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3-(Bromomethyl)-5-chlorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Chloro-5-(hydroxymethyl)benzamide | HCID 58962976 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(Bromomethyl)-5-chlorobenzamide | HCID 68661645 | — |
Reaction Steps
(Step 2) Triphenylphosphine (1.27 g) was suspended in acetonitrile (50 ml), bromine (0.25 ml) was added, and the suspension was stirred for 30 min. 3-Chloro-5-(hydroxymethyl)benzamide (0.90 g) obtained in Step 1 was added to the reaction mixture, and the mixture was stirred at 85° C. for 2 hr. The reaction solution was quenched with water and extracted with ethyl acetate. The extract was washed with aqueous sodium hydrogen carbonate solution and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was treated by silica gel chromatography (ethyl acetate:hexane=1:1) to give 3-(bromomethyl)-5-chlorobenzamide (0.54 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470859B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-ab3beec7dcf5469a9993f80f73a39ff2 |
| Source note | uspto-grants-2013_06 |