Methyl iodide → (4-Bromophenyl)(butyl)sulfane

4-Bromobenzenethiol (5 g, 26.44 mmol) was added to a solution of sodium methoxide (1.43 g, 26.48 mmol) in 20 ml of anhydrous methanol. The mixture was stirred for 30 min under nitrogen at room temperature and a solution of methyl iodide (4.51 g, 31.77 mmol) in 20 ml anhydrous methanol was then added. The reaction mixture was stirred overnight at room temperature, poured into 2 M of NaOH aqueous solution (30 ml) and extracted three times with ether (3×100 ml ). The combined organic layer was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After removal of solvent, the product was purified by distillation at 117-119° C. (0.5 mmHg) and was isolated in 88.4% (5.72 g) yield.

1. stirringThe reaction mixture was stirred overnight at room temperature
2. extractionextracted three times with ether (3×100 ml )
3. washThe combined organic layer was washed with saturated sodium chloride solution
4. dry with materialdried over anhydrous magnesium sulfate
5. customAfter removal of solvent
6. distillationthe product was purified by distillation at 117-119° C. (0.5 mmHg)
7. customwas isolated in 88.4% (5.72 g)
8. customyield

ORD 기록

ord-7f446ff3ec824f87ab856c6400036cd9

출처 데이터셋

uspto-grants-2008_12

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07459106B2