Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390052Generated: November 1, 2026

Trifluoroacetic acid → HCID 59323238, compound

https://huagongshe.com/reaction/2390052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21355393HCID 21355393—
ProductHCID 59323238HCID 5932323891.1%

Reaction Steps

To 206 mg of 3-isobutyl-1,2,3,4-tetrahydroisoquinoline obtained in Example 20 was added 458 mg of anhydrous trifluoroacetic acid, followed by stirring at room temperature for 2 hours. Further, 200 mg of anhydrous trifluoroacetic acid was added thereto, followed by stirring at 40° C. for 1 hour. After completion of the reaction, the reaction liquid was concentrated under reduced pressure, added with ethyl acetate, and washed with an aqueous sodium bicarbonate solution and then with brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed by evaporation to obtain 283 mg (yield 91%) of a title compound as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273766B2
Source datasetuspto-grants-2012_09
ORD IDord-dd6ae9f9b50c4c0e8188c5752c0ee00e
Source noteuspto-grants-2012_09