Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfide | HCID 1068 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 2-Fluoro-4-(hydroxymethyl)benzonitrile | HCID 11829631 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Cyano-3-fluorobenzyl bromide | HCID 2778466 | — |
Reaktionsschritte
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 chromatography (silica gel, 5-10% EtOAc/hexane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06297239B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-2fd2548bab09475e9e9d167f92a28e95 |
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| Quellennotiz | uspto-grants-2001_10 |
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