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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl [3-(4-iodoimidazol-1-yl)-1,1-dimethyl-propyl]-carbamate | HCID 59808428 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Iodo-imidazol-1-yl)-1,1-dimethyl-propylamine | HCID 21094545 | 98.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977334B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-f5999c035a1d49de86e459abc2d40ec3 |
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| Source note | uspto-grants-2011_07 |
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