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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168418Generated: November 1, 2026

(1-Ethoxycyclopropoxy)trimethylsilane → HCID 67126828, compound

https://huagongshe.com/reaction/2168418

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 415B (0.633 g) and (1-ethoxycyclopropoxy)trimethylsilane (1.601 ml) in anhydrous methanol (15 mL) and acetic acid (1.7 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% and 10% methanol in dichloromethane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045420B2
Source datasetuspto-grants-2015_06
ORD IDord-f4ca549657d248968e9d1e0d2a8ad44c
Source noteuspto-grants-2015_06