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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651307Generated: November 2, 2026

Phenothiazine → (3-Aminopropyl)triethoxysilane

https://huagongshe.com/reaction/1651307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenothiazineHCID 7108—
ReactantAllylamineHCID 7853—
ReactantTriethoxysilaneHCID 13830—
Product(3-Aminopropyl)triethoxysilaneHCID 1352165%

Reaction Steps

571 parts of allylamine, 0.38 part of [Rh(NBD)2 ](+). BF4(-) (note: NBD: Norbornadiene), 1.0 part of phenothiazine and 1640 parts of triethoxysilane were charged into a sealed tube and allowed to react in an oil bath for 2 hours at 130° C. Following cooling, the product was analyzed with gas chromatography. Aminopropyltriethoxysilane was produced at a yield of 65% and moreover, the ratio of γ:β isomer was 24:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927949
Source datasetuspto-grants-1990_05
ORD IDord-d90c2125541648e1aa53f5c13e51d10e
Source noteuspto-grants-1990_05