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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010579Generated: October 25, 2026

Trifluoroacetic acid → 3-(4-Iodo-imidazol-1-yl)-1,1-dimethyl-propylamine

https://huagongshe.com/reaction/1010579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl [3-(4-iodoimidazol-1-yl)-1,1-dimethyl-propyl]-carbamateHCID 59808428—
SolventDichloromethaneHCID 6344—
Product3-(4-Iodo-imidazol-1-yl)-1,1-dimethyl-propylamineHCID 2109454598.2%

Reaction Steps

10 mL (130 mmol) trifluoroacetic acid were added to a solution of 1.90 g (5.00 mmol) tert-butyl [3-(4-iodo-imidazol-1-yl)-1,1-dimethyl-propyl]-carbamate in 90 mL dichloromethane at ambient temperature with vigorous stirring. The reaction mixture was stirred for 16 h at ambient temperature and the solvent was eliminated using the rotary evaporator. The residue was taken up in 100 mL sodium hydroxide solution (1M) and 100 mL dichloromethane. The phases were separated and the aqueous phase was extracted three times with 100 mL dichloromethane. The combined organic phases were dried over magnesium sulphate and the solvent was eliminated using the rotary evaporator. 1.37 g (4.91 mmol, 98%) 3-(4-iodo-imidazol-1-yl)-1,1-dimethyl-propylamine were obtained as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977334B2
Source datasetuspto-grants-2011_07
ORD IDord-f5999c035a1d49de86e459abc2d40ec3
Source noteuspto-grants-2011_07