HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (4-Bromo-3-methylphenyl)(methyl)sulfane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-3-methylbenzene-1-thiol | HCID 15661105 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (4-Bromo-3-methylphenyl)(methyl)sulfane | HCID 26370189 | 99.5% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 4-bromo-3-methylbenzenethiol (5.47 g, 26.9 mmol) in DMF (25 mL) was added NaH (0.743 g, 32.3 mmol) at RT. After 15 minutes at RT, the solution was cooled to 0° C. and iodomethane (2.02 ml, 32.3 mmol) was added. The cooling bath was removed and the mixture was allowed to warm up to RT. After 1 hour, water was added and the mixture was extracted with EtOAc (3×). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated to give 5.81 g of (4-bromo-3-methylphenyl)(methyl)sulfane as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101612B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-681b44b80a914c4ea9a700a725aa2305 |
| Source note | uspto-grants-2012_01 |