Ammonium Chloride → 1,2-Bis(2-chloro-5-methoxyphenyl)disulfane

To a solution of 2-bromo-1-chloro-4-methoxybenzene (4.42 g, 19.9 mmol) in THF stirring at −10° C. under nitrogen was added isopropylmagnesium chloride (9.9 mL, 19.9 mmol, 2M in THF). The reaction was allowed to warm to ambient temperature stirred for 4 hours. The reaction was cooled to −40° C. and zinc(II) chloride (19.9 mL, 19.9 mmol, 1M in ether) was added and the solution stirred for minutes. The reaction was cooled to −78° C. and sulfurothioyl dichloride (0.80 mL, 9.9 mmol) was added. After stirring for 15 minutes at −78° C., saturated NH4Cl was added and the mixture was warmed to ambient temperature and extracted multiple times with EtOAc. The combined organic layers were dried with sodium sulfate, filtered, and concentrated to give a residue which was purified by silica chromatography (10% EtOAc in hexanes) to afford the title compound (1.52 g, 21.9% yield).

1. temperatureThe reaction was cooled to −40° C.
2. stirringthe solution stirred for minutes
3. temperatureThe reaction was cooled to −78° C.
4. stirringAfter stirring for 15 minutes at −78° C.
5. temperaturethe mixture was warmed to ambient temperature
6. extractionextracted multiple times with EtOAc
7. dry with materialThe combined organic layers were dried with sodium sulfate
8. filtrationfiltered
9. concentrationconcentrated
10. customto give a residue which
11. customwas purified by silica chromatography (10% EtOAc in hexanes)

ORD record

ord-ca638dfc4ebc4b61a90b814a9c546475

Source dataset

uspto-grants-2014_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08883828B2