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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216234Generated: October 25, 2026

Trimethoxysilane → 4,5-Dimethoxy-2-nitrobenzyl 6-(trimethoxysilyl)hexyl ether

https://huagongshe.com/reaction/2216234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethoxysilaneHCID 17215—
Reactant5-Hexenyl 4,5-dimethoxy-2-nitrobenzyl etherHCID 21941037—
CatalystPlatinic chloride hexahydrateHCID 134756—
Product4,5-Dimethoxy-2-nitrobenzyl 6-(trimethoxysilyl)hexyl etherHCID 2194107934%

Reaction Conditions

Temperature37 °C

Reaction Steps

A 20-ml eggplant type flask was purged with nitrogen, and charged with 2.95 g (10.0 mmol) of 5-hexenyl 4,5-dimethoxy-2-nitrobenzyl ether, 1.47 g (12 mmol) of trimethoxysilane, and an infinitesimal amount of hydrogen hexachloroplatinate(IV) hexahydrate (H2PtCl6·6H2O), followed by stirring at 37° C. for 30 minutes. Thereafter, the bath temperature was raised to 100° C., and the reaction was completed in 2 hours. The reaction mixture was purified by silica gel column chromatography using a medium-pressure column. Using a mixture of hexane, ethyl acetate and tetramethoxysilane (in a volume ratio of 100:20:1) as the eluent, 1.4 g (3.35 mmol) of the desired product was obtained in a 34% yield. Its Rf value (for the aforesaid eluent) was 0.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112397B2
Source datasetuspto-grants-2006_09
ORD IDord-e216d9f937914b04ab8c2a7b83608be9
Source noteuspto-grants-2006_09