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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725097Generated: November 2, 2026

Trifluoroacetic acid → H-L-Ile-D,L-Pip-OBzl TFA

https://huagongshe.com/reaction/1725097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBoc-L-Ile-DL-Pip-OBzlHCID 131724669—
ProductH-L-Ile-D,L-Pip-OBzl TFAHCID 131724670—

Reaction Steps

Boc-L-Ile-DL-Pip-OBzl (3.33 g, 7.70 mmol) was dissolved in TFA (10 ml) and left with standing on ice for 30 minutes. On completion of the reaction, TFA was removed by evaporation, and the residue was vacuum-dried to obtain H-L-Ile-DL-Pip-OBzl.TFA. The compound was dissolved in DMF (16 ml), and Boc-D-Tyr(Me)-OH (3.41 g, 11.6 mmol) was then added. HBTU (4.38 g, 11.6 mmol), HOBt.H2O (1.18 g, 7.70 mmol), and triethylamine (7.01 ml, 50.1 mmol) were further added and stirred for 3 hours under ice-cooling. The reaction solution was concentrated, dissolved in ethyl acetate, and successively washed with an aqueous 10% citric acid solution, an aqueous 4% sodium bicarbonate solution, and saturated saline. The product was dried over MgSO4 and concentrated, and the resulting foam substance was purified by flash silica gel chromatography (4×30 cm, 1% methanol/chloroform) to obtain the foam title diastereomer mixture (3.46 g, 5.67 mmol, 74% yield). TLC: Rf=(CHCl3/MeOH=9/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488712B2
Source datasetuspto-grants-2009_02
ORD IDord-52f725c8f0cd46b7b76f0a59bc34cdfb
Source noteuspto-grants-2009_02