Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082106Generated: October 25, 2026

1,1-Dichloro-1-fluoromethanesulfenyl chloride → 1-(2,6-Dichloro-4-trifluoromethylphenyl)-2,5-dimethyl-3-(dichlorofluoromethylthio)pyrrole

https://huagongshe.com/reaction/2082106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dichloro-1-fluoromethanesulfenyl chlorideHCID 75926—
Reactant1-(2,6-Dichloro-4-trifluoromethylphenyl)-2,5-dimethylpyrroleHCID 22418322—
SolventDichloromethaneHCID 6344—
Product1-(2,6-Dichloro-4-trifluoromethylphenyl)-2,5-dimethyl-3-(dichlorofluoromethylthio)pyrroleHCID 2241832890%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 3.00 g (9.74 mmoles) of the 1-(2,6-dichloro-4-trifluoromethylphenyl)-2,5-dimethylpyrrole prepared above in 60 mL of dichloromethane was added dropwise 1.03 mL (1.67 g, 9.86 mmoles) of dichlorofluoromethanesulfenyl chloride in 5 mL of dichloromethane solution. The mixture was maintained at 0° C. for 3 hours and then washed with a saturated aqueous solution of NaHCO3. Removal of solvent under reduced pressure afforded a black oil which was chromatographed on silica gel with a 1% EtOAc in hexane eluent to give 3.85 g (90%) of 1-(2,6-dichloro-4-trifluoromethylphenyl)-2,5-dimethyl-3-(dichlorofluoromethylthio)pyrrole as a yellow oil: 1H NMR (CDCl3): δ2.00 (s, 3H), 2.10 (s, 3H), 6.27 (s, 1H), 7.80 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187185
Source datasetuspto-grants-1993_02
ORD IDord-116897f08c4645019cd2a3bde98529d6
Source noteuspto-grants-1993_02