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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448808Generated: November 1, 2026

Trifluoroacetic acid → HCID 20375745, compound

https://huagongshe.com/reaction/1448808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 20375747HCID 20375747—
SolventAnisoleHCID 7519—
ProductHCID 20375745HCID 20375745—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 16.5 g of methyl 3-(p-methoxybenzyloxycarbonylamino)-1,5-cyclohexadienecarboxylate in 40 ml of anisole at about 25° C. is added slowly 30 ml of trifluoroacetic acid. After the addition of the first 5 ml the solid dissolves. The solution is cooled in a ice bath and the addition of trifluoroacetic acid continues. The solution is maintained at 0° C. for one hour, then the solvents are removed in vacuo (1 mm) maintaining the temperature below 40° C. The resulting oily residue is cooled to 0° C. and anhydrous ether added with stirring. The precipitate is filtered off to give 8.1 g of methyl 3-amino-1,5-cyclohexadienecarboxylate trifluoroacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04187316
Source datasetuspto-grants-1980_02
ORD IDord-d169a170d084436da7d5a967da676617
Source noteuspto-grants-1980_02