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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897840Generated: November 1, 2026

Trifluoroacetic acid → HCID 58399742, compound

https://huagongshe.com/reaction/1897840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 67236634HCID 67236634—
SolventEthyl AcetateHCID 8857—
ProductHCID 58399742HCID 58399742—

Reaction Steps

To the resulting tert-butyl 2-[4-(3,4-bis(tert-butoxycarbonylamino)thien-2-yl)phenyl]-4-tert-butoxycarbonylaminothien-3-ylcarbamate was added 80 equivalents of trifluoroacetic acid, and a reaction was performed at 25° C. for 3 hours. The resulting reaction liquid was dropped slowly to a saturated aqueous sodium carbonate solution to neutralize, thereby stopping the reaction. Ethyl acetate was added to the reaction liquid and stirred, and then the organic layer was taken and the solvent was distilled off, and the residue was purified by silica gel column chromatography using an ethyl acetate/hexane solvent, so that 2-[4-(3,4-diaminothien-2-yl)phenyl]thiophene-3,4-diamine was obtained. The yield based on the charged tert-butyl 2-[4-(3,4-bis(tert-butoxycarbonylamino)thien-2-yl)phenyl]-4-tert-butoxycarbonylaminothien-3-ylcarbamate was 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519150B2
Source datasetuspto-grants-2013_08
ORD IDord-fa59dfdbe3df4ebfa96f9873de29ca1b
Source noteuspto-grants-2013_08