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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291753Generated: October 31, 2026

Trifluoroacetate → HCID 178446000, compound

https://huagongshe.com/reaction/2291753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetateHCID 84468—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantH-Arg(NO2)Leu-NH2HCID 178446021—
SolventDimethylformamideHCID 6228—
ProductHCID 178446000HCID 178446000—

Reaction Steps

443 g of trifluoroacetate of H-Arg(NO2)Leu-NH2 are dissolved in 2 l of DMF. 200 g of Boc-Ala-OH, then 500 g of BOP are added. The pH is adjusted to 7 with pH paper (on small samples of the reaction medium) with the aid of NEM. The medium is stirred and the development of the reaction is followed by TLC. The reaction is terminated after 4 hrs. The medium is evaporated to dryness in vacuo at 25° C. The residue is taken up in 2 l of water and 2 l of ethyl acetate. The organic phase is washed with a 5% aqueous solution of NaHCO3, with water, dried and evaporated. The tripeptide is recrystallized in ethyl acetate/ether, and finally dried in vacuo. It is monitored by TLC and NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797469
Source datasetuspto-grants-1989_01
ORD IDord-7dd267c0149440208ace6446883252ff
Source noteuspto-grants-1989_01