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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051976Generated: November 4, 2026

(3-Aminopropyl)triethoxysilane → HCID 131736108, compound

https://huagongshe.com/reaction/1051976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Aminopropyl)triethoxysilaneHCID 13521—
ReactantSodium SulfideHCID 14804—
Reactant2-Chloroethyl isocyanateHCID 16035—
SolventEthanolHCID 702—
ProductHCID 131736108HCID 13173610896.7%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388201B2
Source datasetuspto-grants-2016_07
ORD IDord-293ea054bbcb41a2a6c27716753c2af0
Source noteuspto-grants-2016_07