Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535789Generated: October 25, 2026

Water → 1-(Benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene

https://huagongshe.com/reaction/535789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant(E)-1-(Benzyloxy)-4-(2-nitrovinyl)benzeneHCID 5702926—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product1-(Benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzeneHCID 6662909826%

Reaction Steps

Trimethylsulfoxonium iodide (0.62 g, 2.82 mmol) was added in portions to a solution of t-BuOK (0.32 g, 2.82 mmol) in dry DMSO (5 mL). After 10 min a solution of 1-(benzyloxy)-4-[(E)-2-nitrovinyl]benzene (0.60 g, 2.35 mmol) in DMSO (5 mL) was transferred via canula and the mixture was stirred at room temperature for 6 h. The reaction was poured over water (10 mL) and extracted with Et2O (3×10 mL); the organic layers were washed with brine (2×15 mL), dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the residual orange oil was purified by column chromatography on silica gel (5% EtOAc/hexanes) affording 0.16 g of 1-(benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene[Rf=0.5 (20% EtOAc/hexanes), white solid, 26% yield].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859555B2
Source datasetuspto-grants-2014_10
ORD IDord-80f44977588544c69a34aae51756196e
Source noteuspto-grants-2014_10