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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484005Generated: October 30, 2026

Triethylamine → HCID 13561799, compound

https://huagongshe.com/reaction/1484005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBoc-L-ValineHCID 83693—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantBenzyl 2-aminoacetate hydrochlorideHCID 11701227—
SolventDichloromethaneHCID 6344—
ProductHCID 13561799HCID 1356179990.5%

Reaction Steps

Boc-Val-OH (8.69 g, 40.0 mmol) and Gly-OBzl.HCl (8.07 g, 40.0 mmol) were dissolved in methylene chloride (100 ml), and the solution was kept at 0° C. Triethylamine (6.13 ml, 44.0 mmol), HOBt (1-hydroxybenzotriazole, 6.74 g, 44.0 mmol) and WSC.HCl (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, 8.44 g, 44.0 mmol) were added to the solution, and the mixture was stirred overnight at room temperature. The reaction solution was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate (200 ml). The solution was washed with water (50 ml), 5% of citric acid aqueous solution (50 ml× twice), saturated brine (50 ml), 5% of sodium hydrogen carbonate aqueous solution (50 ml× twice), and saturated brine (50 ml) again. The organic layer was dried over anhydrous magnesium sulfate, 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 Boc-Val-Gly-OBzl (13.2 g, 36.2 mmol) as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09420813B2
Source datasetuspto-grants-2016_08
ORD IDord-d8fdeacbaba848dda00ffe77d50342b5
Source noteuspto-grants-2016_08