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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966166Generated: October 29, 2026

Nitrogen → 1-(3-[Tert-butyl(diphenyl)silyl]oxycyclobutyl)ethanone

https://huagongshe.com/reaction/1966166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant3-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylcyclobutanecarboxamideHCID 86634349—
ReactantHCID 178418373HCID 178418373—
SolventDiethyl EtherHCID 3283—
Product1-(3-[Tert-butyl(diphenyl)silyl]oxycyclobutyl)ethanoneHCID 66824288—

Reaction Steps

A solution of 3-[tert-butyl(diphenyl)silyl]oxy-N-methoxy-N-methylcyclobutanecarboxamide (0.7 g, 0.002 mol) in ether (10 mL) was added into 3.0 M of methylmagnesium iodide in ether (3 mL) slowly under N2. The reaction was stirred and heated to reflux for 2 h. The mixture was quenched with ice and the ether layer separated. The aq. layer was acidified with 1N HCl and extracted several times with ether. The organic layers were combined, dried over MgSO4, concentrated and purified with Combiflash (silica gel, 0-30% EtOAc/Hex) to give the desired product (0.6 g) as colorless oil. LCMS calculated for C22H29O2Si(M+H)+: 353.2. Found: 353.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-db5d2869f40d411098eda4a003fe5fdb
Source noteuspto-grants-2013_04