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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246913Generated: October 28, 2026

Trifluoroacetate → HCID 178462179, compound

https://huagongshe.com/reaction/246913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetateHCID 84468—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 178418600HCID 178418600—
SolventDimethylformamideHCID 6228—
ProductHCID 178462179HCID 178462179—

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°. 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 numberUS04704450
Source datasetuspto-grants-1987_11
ORD IDord-be3c7ea898e04beda97c7de9a7faf593
Source noteuspto-grants-1987_11