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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045225Generated: November 1, 2026

(1-Ethoxycyclopropoxy)trimethylsilane → HCID 67126828, compound

https://huagongshe.com/reaction/1045225

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 numberUS08563735B2
Source datasetuspto-grants-2013_10
ORD IDord-3a005c35e616491b922aec70fa0b1f0e
Source noteuspto-grants-2013_10