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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9583Generated: October 26, 2026

Dicyclohexylcarbodiimide → HCID 178418733, compound

https://huagongshe.com/reaction/9583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-Trifluoromethyl-1,2-phenylenediamineHCID 520822—
Reactant4-Bromo-2-fluorophenylisothiocyanateHCID 2757003—
SolventDichloromethaneHCID 6344—
ProductHCID 178418733HCID 178418733—

Reaction Conditions

Temperature45 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091228B2
Source datasetuspto-grants-2006_08
ORD IDord-66414de28ead4eef90b6009cd06980d8
Source noteuspto-grants-2006_08