HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051973Generated: October 31, 2026
(3-Aminopropyl)triethoxysilane → HCID 58903422, compound
https://huagongshe.com/reaction/1051973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58903422 | HCID 58903422 | 105.3% |
Reaction Steps
3-Aminopropyltriethoxysilane (132.82 g, 0.60 mol, 1.00 eq) is initially charged in ethanol (300 ml) in a three-neck flask with precision glass stirrer, internal thermometer, dropping funnel and reflux condenser, and cooled to −78° C. 2-Chloroethyl isocyanate (63.34 g, 0.60 mol, 1.00 eq) is added dropwise at −78 to −68° C. within 1.75 h and then the mixture is heated to 50° C. Potassium thioacetate (68.53 g, 0.60 mol, 1.00 eq) is added in five portions and the mixture is heated to reflux. After a reaction time of 2.25 h, the mixture is cooled to room temperature and the suspension is filtered. The filtrate is freed of the solvent on a rotary evaporator and dried under reduced pressure. The (EtO)3Si—CH2CH2CH2—NH—CO—NH—CH2CH2—S—CH3 product (213.91 g, 97.3% of theory) is obtained as a waxy white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388200B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-b93823ef77834618a5ec19a36ee90ed6 |
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| Source note | uspto-grants-2016_07 |
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