Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl phenyl sulfoxide | HCID 14516 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Bromomethyl phenyl sulfoxide | HCID 11816834 | — |
Reaction Steps
Methyl phenyl sulfoxide (21.644 g, 154.4 mmol) was dissolved in anhydrous pyridine (27.4 mL, 2.2 eq) and dry acetonitrile (100 mL). The solution was cooled to −40° C. under an argon atmosphere. A solution of bromine (49.4 g, 2eq) in dry acetonitrile (50 mL) was added slowly, maintaining the same temperature. The mixture was stirred at −40° C. for 1 h and then overnight at room temperature. The solvent was evaporated under vacuum and the residue was dissolved in dichloromethane. The organic layer was washed with Na2S2O3 20%, dried over anhydrous Na2SO4 and concentrated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359294B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-25d1c1c5829e486987395f9885efaa5f |
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| Source note | uspto-grants-2016_06 |
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