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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033504Generated: November 1, 2026

Trifluoroacetic acid → HCID 10362064, compound

https://huagongshe.com/reaction/1033504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantO-BenzylhydroxylamineHCID 102313—
ReactantHCID 10061627HCID 10061627—
SolventTolueneHCID 1140—
ProductHCID 10362064HCID 1036206477.5%

Reaction Steps

Trifluoroacetic acid (17.4 g) was added in one portion to a solution of 5,6,7,8-tetrahydro-5-methyl-2-(phenylmethoxy)-quinolin-5-ol (41 g), phenylmethoxyamine (47 g), and toluene (770 ml) at room temperature. The solution was stirred at room temperature for 24 hrs, and then quenched with concentrated ammonium hydroxide solution. The layers were separated and the aqueous phase was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over potassium carbonate, filtered, and the filtrate was concentrated. Purification by high performance liquid chromatography (silica gel, elution with ethyl acetate-hexanes) gave 44.2 g (77%) of 5,6,7,8-tetrahydro-5-methyl-N,2-bis(phenylmethoxy)-5-quinolinamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310914
Source datasetuspto-grants-1994_05
ORD IDord-e5d193cd859a46cc963d998cc1f6e312
Source noteuspto-grants-1994_05