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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439591Generated: October 29, 2026

Trifluoroacetic acid → HCID 22860941, compound

https://huagongshe.com/reaction/439591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBoc-L-ValineHCID 83693—
ReactantHCID 15138263HCID 15138263—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22860941HCID 2286094175%

Reaction Steps

A 500 mL round bottom flask was charged with 46.52 g (99 mmol) N-tert-Butyloxycarbonyl-L-leucinyl-L-phenylalanine benzyl ester, 340 mL anhydrous m ethylene chloride (CH2Cl2), and 51 mL trifluoroacetic acid (TFA). The mixture was stirred at room temperature under a nitrogen atmosphere for 3 hours, and then concentrated in vacuo. The residue was azeotroped twice with toluene, and carried on. The same 500 mL round bottom flask containing the crude TFA salt was placed under a nitrogen atmosphere and charged with 21.5 g (99 mmol) Boc-L-valine, 13.4 g (99 mmol) HOBT, and 270 mL anhydrous THF The solution was cooled in an ice/acetone bath and 21.4 a (104 mmol) DCC was added in one portion. The mixture was stirred in the cold for 1 hour, and then warmed to room temperature and stirred overnight. The precipitated DCU was filtered off, and the filtrate was concentrated in vacuo. The residue was taken up in ethyl acetate and washed once with water, once with a 10% solution off citric acid, once with saturated NaHCO3, and once with brine. The organic layer was then dried over Na2SO4, filtered, and concentrated in vacuo. The resultant solid was precipitated from ethanol with H2O to provide 41.96 g (75%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514778
Source datasetuspto-grants-1996_05
ORD IDord-3493c8c6b2d045228155bb306ba2cb11
Source noteuspto-grants-1996_05