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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044647Generated: October 31, 2026

Trifluoroacetic acid → HCID 59537065, compound

https://huagongshe.com/reaction/1044647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-MethylmorpholineHCID 7972—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantHCID 131730908HCID 131730908—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59537065HCID 59537065—

Reaction Steps

To a cold (−15° C.) solution of Boc-Ala-OH (118 mg, 0.63 mmol) and NMM (103 μl, 1.03 mmol) in THF (8 mL) was added ECF (61 μl, 0.64 mmol) and stirred vigorously. After 2 min. a solution of the TFA salt of Ala-Ala-NH(CH2)4—Br (280 mg, 0.69 mmol) in a mixture of THF:DMF (4 mL:2 mL) was added to it followed by NMM (170 μL, 1.7 mmol) and stirred for further 30 minutes. The mixture was warmed to r.t. and stirred for 6 h. The solvent was removed under reduced pressure to give a residue which was diluted with EtOAc and washed with saturated citric acid, saturated NaHCO3 and the organic layer was dried over Na2SO4 and concentrated under vacuum to give a residue, which was purified by silica gel flash column chromatography (EtOAc:Hexanes—9:1) to give the desired product as a solid (m.p.—196-198° C.) in moderate yields (137 mg, 54%). TLC (MeOH:DCM—1:9; Rf—0.53).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563686B2
Source datasetuspto-grants-2013_10
ORD IDord-87bd37313afa4921bfde1344ea71df7b
Source noteuspto-grants-2013_10