HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199266Generated: October 27, 2026
Acetylglycine → (N-Acetyl-glycylpropyl)triethoxysilane
https://huagongshe.com/reaction/2199266
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | (3-Iodopropyl)triethoxysilane | HCID 11782516 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (N-Acetyl-glycylpropyl)triethoxysilane | HCID 56943229 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09358200B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-158a6bd750394d5fb9f53c9dc8a421f2 |
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| Source note | uspto-grants-2016_06 |
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