HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051976Generated: November 4, 2026
(3-Aminopropyl)triethoxysilane → HCID 131736108, compound
https://huagongshe.com/reaction/1051976
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131736108 | HCID 131736108 | 96.7% |
Reaction Steps
In a first reaction step, 3-aminopropyltriethoxysilane (159.39 g, 0.72 mol, 1.00 eq) is initially charged in ethanol (3.0 l) in a 4 l three-neck flask with precision glass stirrer, internal thermometer, dropping funnel and reflux condenser, and cooled to −78° C. 2-Chloroethyl isocyanate (75.92 g, 0.72 mol, 1.00 eq) is added dropwise at −78 to −69° C. within 2.25 h and then the mixture is heated to 50° C. Dry sodium sulphide (Na2S, 28.09 g, 0.36 mol, 0.50 eq) is added in five portions and the mixture is heated to reflux. After a reaction time of 4.5 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—CH2CH2—NH—CO—NH—CH2CH2CH2—Si(OEt)3 product (214.09 g, 96.7% of theory) is obtained as a waxy, white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388201B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-293ea054bbcb41a2a6c27716753c2af0 |
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| Source note | uspto-grants-2016_07 |
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