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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1432753Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1432753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktWaterHCID 962—
Edukt[5-(2,6-Dichloro-4-trifluoromethylphenyl)-2-nitrophenyl]isopropyl sulfideHCID 22170887—
EduktHCID 178460720HCID 178460720—
KatalysatorIronHCID 23925—
LösungsmittelTolueneHCID 1140—
Produkt4-(2,6-Dichloro-4-trifluoromethylphenyl)-2-isopropylthioanilineHCID 2217093036%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07612105B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-be6d3dc079f44baebf149b67aa51558b
Quellennotizuspto-grants-2009_11