HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110195Generated: November 1, 2026
Trifluoroacetic acid → HCID 86747957, compound
https://huagongshe.com/reaction/1110195
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86747957 | HCID 86747957 | — |
Reaction Steps
The peptide is eliminated from the resin by treatment with about 10 ml of a (90:5:5) mixture of trifluoroacetic acid, water and 1,2-ethanedithiol for 8 minutes; the reaction mixture is filtered, the filtrate is concentrated under reduced pressure, and the peptide is precipitated with a 1:1 mixture of diisopropyl ether and hexane and dried. The abovementioned treatment with trifluoroacetic acid/water/1,2-ethanedithiol itself results in partial elimination also of the trityl groups (where present) and the tert.-butyl group. This elimination is completed by heating the peptide precipitate in trifluoroacetic acid/water/1,2-ethanedithiol (90:5:5) at 30° C., for 30 minutes. The resulting crude products from the syntheses with and without trityl protective groups are investigated by HPLC (column: Nucleosil 5C18, 250×4.6 mm; mobile phase: A=0.1% trifluoroacetic acid in water; B=0.1% trifluoroacetic acid in acetonitrile. Gradient: 0 to 40% B in 30 minutes; flow rate: 1 ml/minute. Detection: 215 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05324833 |
|---|
| Source dataset | uspto-grants-1994_06 |
|---|
| ORD ID | ord-bf48d4c75be643b483a0254a31dfa87c |
|---|
| Source note | uspto-grants-1994_06 |
|---|