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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771022Generated: November 1, 2026

Hydrochloric Acid → t-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoate

https://huagongshe.com/reaction/1771022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant5-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acidHCID 17989820—
SolventEthyl AcetateHCID 8857—
Productt-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoateHCID 9003454489%

Reaction Steps

Triethylamine (2.22 g; 22.0 mmol) was added dropwise to a stirred solution of 5-(Boc-amino)-4-oxopentanoic acid (4.62 g; 20.0 mmol) and t-butyl bromoacetate (4.30 g; 22.0 mmol) in ethyl acetate (60 mL) under argon at ambient temperature. The mixture (slurry) was refluxed for 17 h, then cooled to ambient temperature, poured into 0.5 M HCl (100 mL) and shaken thoroughly. The aqueous portion was extracted with ethyl acetate (2×20 mL). The combined organic solutions were washed with saturated NaHCO3 solution (1×20 mL) and saturated NaCl solution (1×20 mL) then dried (MgSO4), filtered and evaporated. Evaporation resulted in an amber oil that was purified by flash chromatography on a 40×55-mm silica gel 60 column eluted with ethyl acetate-hexane (1:1) (600 mL), collecting 5×100 mL fractions. Evaporation of fractions 1 and 2 resulted in 6.15 g (89%) product (yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249086B2
Source datasetuspto-grants-2016_02
ORD IDord-043ee78e928c4da7b67a8a64d9a49c80
Source noteuspto-grants-2016_02