HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956739Generated: October 29, 2026
Trifluoroacetic acid → HCID 131720770, compound
https://huagongshe.com/reaction/1956739
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 12991453 | HCID 12991453 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131720770 | HCID 131720770 | — |
Reaction Steps
BOC-N(Et)Gly-(L)-Asp(OBzl)-(L)-Cha-NH2 is dissolved in dichloromethane (~1:12 wt/wt), and to that solution is added TFA at ambient temperature. This is then stirred until HPLC indicates complete reaction (3-5 hours). The solution is concentrated to about 1/2 volume at 40°-45° C. To this warm solution is added MTBE (~1:10 wt/wt vs. BOC-N(Et)Gly-(L)-Asp(OBzl)-(L)-Cha-NH2) while maintaining the temperature >40° C. The mixture is slowly cooled to about 5° C. and stirred for 1 hour to ensure complete crystallization. The resulting solids are filtered, and washed with chilled MTBE. The solids are dried under reduced pressure and analyzed for content of TFA·N(Et)Gly-(L)-Asp(OBzl)-(L)-Cha-NH2 (HPLC wt/wt assay). Yield is generally nearly quantitative, purity >95 A %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780590 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-9ab17e96c5c2401cae94cf58eca17c4c |
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| Source note | uspto-grants-1998_07 |
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