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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023817Generated: November 3, 2026

Water → 1-((2-Methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene

https://huagongshe.com/reaction/1023817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant(E)-1-((2-methoxyethoxy)methoxy)-4-(2-nitrovinyl)benzeneHCID 67064875—
SolventDimethyl SulfoxideHCID 679—
Product1-((2-Methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzeneHCID 6706487657.6%

Reaction Steps

Trimethylsulfoxonium iodide (0.76 g, 3.44 mmol) was added in small portions to a suspension of NaH 0.14 g (60% in mineral oil), 3.44 mmol] in dry DMSO (5 mL). The mixture was stirred until gas evolution ceased and a clear solution was formed (45 min). Then, a solution of (E)-1-((2-methoxyethoxy)methoxy)-4-(2-nitrovinyl)benzene (Intermediate J, 0.73 g, 2.86 mmol) in DMSO (5 mL) was transferred via cannula and the reaction was stirred for additional 20 h. The mixture was poured into water (20 mL) and extracted with Et2O (3×15 mL). The organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and filtered; after removal of the solvent, the residual orange oil was purified by column chromatography on silica gel (10-20% EtOAc/Hexanes) affording 0.44 g of 1-((2-methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene [Rf=0.4 (50% AcOEt/Hexanes), colorless oil, 36% yield].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722743B2
Source datasetuspto-grants-2014_05
ORD IDord-70900e6eaf61436e81bcc51081826685
Source noteuspto-grants-2014_05