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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477593Generated: October 30, 2026

O-Xylene → Allylamine

https://huagongshe.com/reaction/477593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantAllylamineHCID 7853—
ReactantTriethoxysilaneHCID 13830—
CatalystTetrarhodium dodecacarbonylHCID 9940312—
ProductAllylamineHCID 7853—
ProductHCID 10236113HCID 10236113—

Reaction Conditions

Temperature110 °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, charged with 1.9 milligrams of tetrarhodium dodecacarbonyl (2.5×10-6 mole), 14 grams of allylamine (0.25 mole) and 60 ml. of xylene, and heated in an oil bath maintained at a temperature of 110° C. Thereafter, 41 grams of triethoxy silane (0.25 mole) was dropwise added to the mixture from the dropping funnel over 30 minutes. The reaction was continued at a temperature of 110° C. for 2 hours under stirring and CO flush. It was revealed by gas chromatography that gamma-aminopropyl triethoxy silane was obtained in a yield of 58% on an allylamine basis, while the yield of beta-aminopropyl triethoxy silane was 4.9% on an allylamine basis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888436
Source datasetuspto-grants-1989_12
ORD IDord-78d8e2008711425196d5393550c8313f
Source noteuspto-grants-1989_12