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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440405Generated: October 31, 2026

Trifluoroacetic acid → HCID 53766859, compound

https://huagongshe.com/reaction/1440405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 53846502HCID 53846502—
SolventChloroformHCID 6212—
ProductHCID 53766859HCID 53766859—

Reaction Steps

To a solution, being ice cool, ed, of N-tert-butoxycarbonyl-(L)-isoleucyl-(L)-tryptophanol (1.0 g) in chloroform (10 ml), trifluoroacetic acid (5%, 0.5 g) was added, followed by stirring at the same temperature for 4 hours. After the reaction mixture was concentrated under reduced pressure, ethyl acetate was added to the residue. The ethyl acetate layer was washed with water and dried (MgSO4), and the solvent was distilled off to yield (L)-isoleucyl-(L)-tryptophanol as an oily substance. This oily substance was dissolved in chloroform (20 ml), and p-toluenesulfonyl chloride (0.52 g) was added and then triethylamine (1.4 ml) was added at 0° C. After stirring at room temperature for 2 days, the reaction mixture was poured over water and extracted with chloroform. After the chloroform layer was dried (MgSO4), the solvent was distilled off, and the oily residue was recrystallized from ethyl acetate to yield N-(p-toluenesulfonyl)-(L)-isoleucyl-(L)-tryptophanol (0.32 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498728
Source datasetuspto-grants-1996_03
ORD IDord-701eb29eaa554a74901015a60347af94
Source noteuspto-grants-1996_03