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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735022Generated: October 26, 2026

Trifluoroacetic acid → 1-(4-Iodophenyl)cyclopropanamine

https://huagongshe.com/reaction/735022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 59019959HCID 59019959—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(4-Iodophenyl)cyclopropanamineHCID 23130221—

Reaction Steps

3 mL (38.76 mmol) of trifluoroacetic acid are added to a solution of 1 g (2.78 mmol) of tert-butyl [1-(4-iodophenyl)cyclopropyl]carbamate in 40 mL dichloromethane and stirred for 24 h. Then the solvent is eliminated by rotary evaporation and the residue is combined with toluene and then again eliminated by rotary evaporation. This residue is then added to a solution of 0.39 g (2.8 mmol) of potassium carbonate in 20 mL of water and stirred for 30 minutes at RT. The aqueous phase is extracted with dichloromethane, the organic phase is dried with sodium sulfate and the solvent is eliminated by rotary evaporation. Yield: 0.7 g (97% of theory); C9H10IN (M=259.09); calc.: molecular ion peak (M+H)+: 260; found: molecular ion peak (M+H)+: 260.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592373B2
Source datasetuspto-grants-2009_09
ORD IDord-9d062bb41e1d459d9318f3d395f08a7a
Source noteuspto-grants-2009_09