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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30898Generated: October 26, 2026

Dicyclohexylcarbodiimide → HCID 178418733, compound

https://huagongshe.com/reaction/30898

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 numberUS07423156B2
Source datasetuspto-grants-2008_09
ORD IDord-96df1c5f8f534faaa5ac531f3060bf4f
Source noteuspto-grants-2008_09