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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797166Generated: October 29, 2026

Trifluoroacetic acid → HCID 22177252, compound

https://huagongshe.com/reaction/1797166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69595261HCID 69595261—
SolventDichloromethaneHCID 6344—
ProductHCID 22177252HCID 2217725295.3%

Reaction Steps

To a stirred solution of (3,5-dichloro-phenyl)-{2-[2-(4-iodophenyl)-pent-4-enylamino]-ethyl}-carbamic acid tert-butyl ester (0.493 g, 0.85 mmol) in CH2Cl2 (20 mL) at 0° C. was added TFA (5 mL). The mixture was stirred and warmed to room temperature for 4 h. The solvent was removed by rotary evaporation and the residue was dissolved in EtOAc and washed twice with NaHCO3 (10% in H2O). The organic extracts were dried over sodium sulfate, filtered and concentrated by rotary evaporation to give N-(3,5-dichloro-phenyl)-N′-[2-(4-iodo-phenyl)-pent-4-enyl]-ethane-1,2-diamine (0.386 g, 0.81 mmol, 95%) as a brown oil. 1H NMR (300 MHz, CDCl3): δ 7.73 (d, 2H), 7.03 (d, 2H), 6.56 (t, 1H), 6.50 (d, 2H), 5.75 (m, 1H), 5.08 (m, 2H), 4.42 (br s, NH), 3.15 (m, 2H), 3.40 (m, 5H), 2.44 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034056B2
Source datasetuspto-grants-2006_04
ORD IDord-b4d161d651144c658f74e4112c65ad6b
Source noteuspto-grants-2006_04