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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216235Generated: October 26, 2026

Trimethoxysilane → 4,5-Methylenedioxy-2-nitrobenzyl 3-(trimethoxysilyl)propyl ether

https://huagongshe.com/reaction/2216235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethoxysilaneHCID 17215—
ReactantAllyl 3,4-methylenedioxy-6-nitrobenzyl etherHCID 21941062—
CatalystPlatinic chloride hexahydrateHCID 134756—
Product4,5-Methylenedioxy-2-nitrobenzyl 3-(trimethoxysilyl)propyl etherHCID 2194103952.4%

Reaction Conditions

Temperature37 °C

Reaction Steps

A 10-ml eggplant type flask was purged with nitrogen, and charged with 1.0 g (4.2 mmol) of allyl 3,4-methylenedioxy-6-nitrobenzyl ether, 0.616 g (5 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, 0.80 g (2.2 mmol) of the desired product was obtained in a 52% 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-8b6f05fc079d4e6cba0e3779d2c364df
Source noteuspto-grants-2006_09