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HRID 9583Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → HCID 178418733, Verbindung

https://huagongshe.com/de/reaction/9583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-Trifluoromethyl-1,2-phenylenediamineHCID 520822—
Edukt4-Bromo-2-fluorophenylisothiocyanateHCID 2757003—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178418733HCID 178418733—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

1,2-Diamino-5-trifluoromethylbenzene (0.50 g, 2.84 mmol) was diluted in dichloromethane (5 mL) and treated with 4-bromo-2-fluoro-phenylisothiocyanate (0.66 g, 2.84 mmol). The dark solution was stirred at 45° C. for 15 minutes, then 1,3-dicyclohexylcarbodiimide (0.44 g, 2.13 mmol) was added all at once. The reaction was heated in a 45° C. oil bath overnight, then cooled and concentrated at reduced pressure. The dark residue was diluted with ethyl acetate, and the organic layer was washed with water. The organic layer was dried (MgSO4) and concentrated in vacuo. The resulting dark brown oil was purified by flash chromatography on silica gel eluted on a gradient from 9:1 hexanes/ethyl acetate to 100% ethyl acetate. The title compound was collected as a light pink solid (0.60 g, 57%). 1H NMR (300 MHz, DMSO-d6) δ 11.3 (broad d, 1H), 9.87 (d, 1H), 7.50 (d, 2H), 7.61 (d, 1H), 7.55–7.41 (m, 3H), 7.35–7.30 (m, 1H); LC/MS m/z 356.2 (MH+), retention time 2.33 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091228B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-66414de28ead4eef90b6009cd06980d8
Quellennotizuspto-grants-2006_08