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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573163Generated: October 30, 2026

(1-Ethoxycyclopropoxy)trimethylsilane → HCID 67126828, compound

https://huagongshe.com/reaction/573163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67126454HCID 67126454—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 67126828HCID 67126828—

Reaction Steps

A solution of EXAMPLE 369B (0.633 g) and (1-ethoxycyclopropoxy)trimethylsilane (1.601 mL) in anhydrous methanol (15 mL) and acetic acid (1.717 mL) was refluxed for 30 minutes and allowed to cool to room temperature. Sodium cyanoborohydride (0.377 g) was then added and the mixture was stirred at ambient temperature overnight. The reaction mixture was concentrated to dryness. The residue was mixed with 5% aqueous Na2CO3 solution (25 mL) and extracted with ethyl acetate. The crude product was purified on a silica gel column eluting with 5% to 10% methanol in dichloromethane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-18136e8c67fb4c5e8e09d1050079d159
Source noteuspto-grants-2015_05