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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477591Generated: October 30, 2026

Allylamine → Allylamine

https://huagongshe.com/reaction/477591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
Reactantcis,cis-1,5-CyclooctadieneHCID 8135—
ReactantTriethoxysilaneHCID 13830—
ReactantHCID 178418416HCID 178418416—
Catalyst19584-30-6HCID 9940312—
SolventO-XyleneHCID 7237—
ProductAllylamineHCID 7853—
ProductHCID 10236113HCID 10236113—

Reaction Conditions

Temperature120 °C

Reaction Steps

A 200 ml. flask equipped with a stirrer, thermometer, dropping funnel, CO inlet tube and reflux condenser having a CO outlet tube, was flushed with carbon monoxide and charged with 1.9 milligrams of tetrarhodium dodecacarbonyl (2.5×10-6 mole), 0.027 gram of 1,5-cyclooctadiene (2.5×10-4 mole) and 60 ml. of xylene. While passing carbon monooxide through the flask at a rate of 10 ml./min., the mixture was heated to a temperature of 120° C. under stirring. To the mixture a mixture of 41 grams of triethoxy silane (0.25 mole) and 14 grams of allylamine (0.25 mole) was dropwise added over a period of 30 minutes. After the addition of the reactants, the reaction was carried out at a temperature of 120° C. for 2.5 hours under CO flush and stirring. It was revealed by gas chromatography that gamma-aminopropyl triethoxy silane was obtained in a yield of 75% on an allylamine basis, while the yield of beta-aminopropyl triethoxy silane was 7.5% on an allylamine basis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888436
Source datasetuspto-grants-1989_12
ORD IDord-5f93aed616cd4f35ab8e5b0357e71d59
Source noteuspto-grants-1989_12