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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417112Generated: November 1, 2026

Silane → HCID 21835995, compound

https://huagongshe.com/reaction/1417112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilaneHCID 23953—
Reactant3-bromopropyltriallylsilaneHCID 11033029—
ReactantHCID 178521474HCID 178521474—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21835995HCID 21835995—

Reaction Steps

Triallyl glycerylpropyl silane was prepared from triallyl bromopropyl silane prepared in Example 7 via glycerol acetonide intermediate. A 250 ml flask equipped with a stir bar was charged with 22.9 grams of 74% triallyl bromopropyl silane reagent (17.0 grams, 62 millimoles of triallyl bromopropyl silane prepared as described in Example 7). The silane was diluted with 175 ml of tetrahydrofuran (commercially available from Aldrich Chemical Co. of Milwaukee, Wis.) containing 1.1 grams (3.2 millimoles) tetrabutylammonium hydrogen sulfate (commercially available from Aldrich Chemical Co.). The reaction vessel was then cooled in an ice bath and purged with nitrogen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05876595
Source datasetuspto-grants-1999_03
ORD IDord-8da50ba171f440b3b74592b8b9bd3c1e
Source noteuspto-grants-1999_03