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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417113Generated: October 29, 2026

Sodium Formate → HCID 21835981, compound

https://huagongshe.com/reaction/1417113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FormateHCID 2723810—
Reactant3-bromopropyltriallylsilaneHCID 11033029—
CatalystTetrabutylammonium BromideHCID 74236—
ProductHCID 21835981HCID 21835981—

Reaction Steps

Triallyl (3-hydroxylpropyl) silane was prepared from triallyl-3-bromopropyl silane prepared in Example 7 via the formyloxypropyl intermediate. A 100 ml flask equipped with stir bar and reflux condenser was charged with 10.0 grams (36 millimoles) of triallyl 3-bromopropyl silane (prepared as described in Example 7), 4.90 grams (72 millimoles) sodium formate (commercially available from Aldrich Chemical Co. of Milwaukee, Wis.) and 0.60 grams of tetrabutyl ammonium bromide (commercially available from Aldrich Chemical Co.). The suspension was stirred at 110° C. for two days. The solution was then filtered and combined with equal volumes of deionized water and cyclohexane (commercially available as Omnisolve from E. Merck of Gibbstown, N.J.). The organic extract was flash chromatographed on silica using first cyclohexane, followed by 80/20 cyclohexane/acetone to collect the triallyl formyloxypropyl silane intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05876595
Source datasetuspto-grants-1999_03
ORD IDord-3e234823c2164ce3a1c59ffc3ca28530
Source noteuspto-grants-1999_03