HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → 4-Cyano-3-fluorobenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-4-(hydroxymethyl)benzonitrile | HCID 11829631 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyano-3-fluorobenzyl bromide | HCID 2778466 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
N-Bromosuccinimide (6.6 g, 0.037 mol) was dissolved in CH2Cl2 (150 mL), cooled to 0° C. and treated with dimethylsulfide (3.27 mL, 0.0446 mol). The solution was cooled to −20° C. and then treated dropwise with a solution of 2-fluoro-4-hydroxymethylbenzonitrile (3.74 g, 0.0248 mol) in CH2Cl2 (30 mL). After the addition, the reaction mixture was stirred at 0° C. for 2 h then left to warm to ambient temperature overnight. The reaction mixture was added to ice/H2O, extracted with EtOAc, the organic layer separated, washed with brine and dried (MgSO4). Filtration and concentration to dryness gave the title compound which was purified by chromatography (silica gel, 5-10% EtOAc/hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-889c81f0543f40ed914e44521fc7a8e3 |
| Source note | uspto-grants-2002_03 |