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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966165Generated: October 31, 2026

Imidazole → 3-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylcyclobutanecarboxamide

https://huagongshe.com/reaction/1966165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant3-hydroxy-N-methoxy-N-methylcyclobutanecarboxamideHCID 18691557—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylcyclobutanecarboxamideHCID 8663434950%

Reaction Steps

Into a solution of 3-hydroxy-N-methoxy-N-methylcyclobutanecarboxamide (0.6 g, 0.004 mol in DMF (10 mL) was added tert-butylchlorodiphenylsilane (3 mL, 0.01 mol), followed by 1H-imidazole (1 g, 0.02 mol). The mixture was stirred at rt over night. The reaction was diluted with dichloromethane and washed with sat. NaHCO3, water and brine. The organic layers were dried over MgSO4, concentrated and purified with Combiflash (silica gel, 0-30% EtOAc/Hex) to give the desired product (0.7 g, 50%) as cis- and trans-isomer mixtures. LCMS calculated for C23H32NO3Si(M+H)+: 398.2. Found: 398.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-53c1818f9999401197c2d1cdccaf2417
Source noteuspto-grants-2013_04