HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862047Generated: October 30, 2026
Trifluoroacetic acid → HCID 53766859, compound
https://huagongshe.com/reaction/862047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 53846502 | HCID 53846502 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 53766859 | HCID 53766859 | — |
Reaction Steps
To a solution, being ice cooled, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05716980 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-f6b4e3358c4f4a4aa81bb57cb5e12ae4 |
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| Source note | uspto-grants-1998_02 |
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