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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965892Generated: October 30, 2026

Triethylamine → HCID 58124406, compound

https://huagongshe.com/reaction/1965892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acidHCID 2734668—
ReactantBenzyl 2-aminoacetate hydrochlorideHCID 11701227—
SolventDichloromethaneHCID 6344—
ProductHCID 58124406HCID 58124406100.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Boc-t-Leu-OH (9.26 g, 40.0 mmol) and Gly-OBzl•HCl (8.06 g, 40.0 mmol) were dissolved in methylene chloride (60 ml), and the solution was maintained at 0° C. Triethylamine (5.60 ml, 40.0 mmol), HOBt (1-hydroxybenzotriazole, 6.75 g, 44.0 mmol), and WSC•HCl (1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride, 8.47 g, 44.0 mmol) were added to the solution, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate (200 ml). The solution was washed with water (50 ml), 5% citric acid aqueous solution (50 ml, twice), saturated brine (50 ml), 5% sodium hydrogencarbonate aqueous solution (50 ml, twice), and saturated brine (50 ml). The organic layer was dried over anhydrous magnesium sulfate, then the magnesium sulfate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to obtain a viscous oily material of Boc-t-Leu-Gly-OBzl (15.20 g, 40.1 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420144B2
Source datasetuspto-grants-2013_04
ORD IDord-d69b1fe756d9490d9880719bf5afd2a7
Source noteuspto-grants-2013_04