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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199266Generated: October 27, 2026

Acetylglycine → (N-Acetyl-glycylpropyl)triethoxysilane

https://huagongshe.com/reaction/2199266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylglycineHCID 10972—
Reactant(3-Iodopropyl)triethoxysilaneHCID 11782516—
ReactantPotassium ethoxideHCID 23670592—
SolventEthanolHCID 702—
Product(N-Acetyl-glycylpropyl)triethoxysilaneHCID 5694322925%

Reaction Steps

A 5 L, 4-neck flask equipped with a heating mantle, a mechanical stirrer, a pot thermometer, an addition funnel, and a short Vigreux column with a distillation head connected to a nitrogen bubbler was charged with 2500 g of ethanol and 146.4 g of N-acetylglycine. This mixture was stirred at room temperature for 15 minutes. 110.5 g of potassium ethoxide were added while maintaining the pot temperature below 50° C. The mixture was heated to a pot temperature of 80° and 362.7 g of 3-iodopropyltriethoxysilane was added. Ethanol was removed by distillation until the pot temperature rose to 90° C. to 95° C. The reaction was followed by GC and heating continued for ˜100 hours until less than 10% of the 3-iodopropyltriethoxysilane remained. The flask and the contents were allowed to cool to room temperature and then filtered to give a clear to slightly hazy solution with 25-30% solids. A sample of solution was stripped of solvent at 120° C. and 1 mm vacuum to remove all solvents and unreacted starting materials. The product was purified by wiped film distillation at 190° C. at 0.5 mm. IR and NMR results were consistent with the target structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09358200B2
Source datasetuspto-grants-2016_06
ORD IDord-158a6bd750394d5fb9f53c9dc8a421f2
Source noteuspto-grants-2016_06