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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635733Generated: October 26, 2026

Acetic Acid → 4-(2,6-Dichloro-4-trifluoromethylphenyl)-2-isopropylthioaniline

https://huagongshe.com/reaction/1635733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactant[5-(2,6-Dichloro-4-trifluoromethylphenyl)-2-nitrophenyl]isopropyl sulfideHCID 22170887—
ReactantHCID 178460720HCID 178460720—
CatalystIronHCID 23925—
SolventTolueneHCID 1140—
Product4-(2,6-Dichloro-4-trifluoromethylphenyl)-2-isopropylthioanilineHCID 2217093036%

Reaction Steps

3.5 g (63.6 mmol) of iron powder, 10 m of water and 1 m of acetic acid were stirred in 20 ml toluene at 60° C. for 30 minutes, and 3.0 g (7.3 mmol) of [5-(2,6-dichloro-4-trifluoromethylphenyl)-2-nitrophenyl]isopropyl sulfide (the compound prepared in Example 8 (2)) in 10 ml toluene was added dropwise. The reaction was carried out with reflux and heating for another 3 hours, and then the reaction mixture was cooled to room temperature. The insolubles were filtered off, and the filtrate was separated with water and toluene. The toluene layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 1.0 g of 4-(2,6-dichloro-4-trifluoromethylphenyl)-2-isopropylthioaniline (yield 36.0%) as a pale yellow dough (nD20 1.5782).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509354B1
Source datasetuspto-grants-2003_01
ORD IDord-20b75dec84324f4d8f5e5beea9cac01e
Source noteuspto-grants-2003_01