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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36560Generated: October 25, 2026

Triethylamine → (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid

https://huagongshe.com/reaction/36560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetic acid, 2-fluoro-, 1,1'-anhydrideHCID 67886—
ReactantN-(tert-butoxycarbonyl)-L-aspartic acidHCID 99718—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
Product(S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acidHCID 10131156—

Reaction Steps

A suspension of Boc-Asp-OH (8.11 mmol) and fluoroacetic anhydride (16.2 mmol) in benzene (30 ml) was treated with triethylamine (16.2 mmol) at room temperature. The catalyst 4-dimethylaminopyridine (0.41 mmol) was added to the solution and the reaction stirred for about 2 h at room temperature. About 100 ml benzene was added to the reaction mixture. The organic solution was washed with 1N HCl (2×50 ml), saturated NaHCO3 (2×50 ml), and saturated NaCl (2×50 ml), followed by drying over anhydrous MgSO4. The solvent was then removed by evaporation under reduced pressure. The resulting oil was applied to a 2.5×80 cm column of silica gel (60-200 mesh). The title compound was eluded with 2% methanol in chloroform.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416013
Source datasetuspto-grants-1995_05
ORD IDord-1f37921e0a2e4e799336bdb217625c12
Source noteuspto-grants-1995_05