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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626316Generated: October 30, 2026

Triphenylphosphine → 1-(1-Cyclopropylethoxy)-2,5-dimethyl-4-nitrobenzene

https://huagongshe.com/reaction/626316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-CyclopropylethanolHCID 79104—
Reactant2,5-Dimethyl-4-nitrophenolHCID 282110—
ReactantSodium BicarbonateHCID 516892—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
SolventTolueneHCID 1140—
Product1-(1-Cyclopropylethoxy)-2,5-dimethyl-4-nitrobenzeneHCID 11762059145.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

3.10 g of Bis(2-methoxyethyl) azodicarboxylate was added to a mixture of 1.70 g of 2,5-dimethyl-4-nitrophenol, 0.88 g of (1-cyclopropyl) ethanol, 3.20 g of triphenylphosphine and 100 mL of toluene at 0° C., and the mixture was stirred at 80° C. for 4 hours. After cooling, a saturated aqueous sodium bicarbonate solution was added, and the mixture was extracted with ethyl acetate, and then the organic layer was washed with water and saturated salt water and dried over anhydrous magnesium sulfate. The resulting residue was subjected to silica gel column chromatography to obtain 1.09 g of 1-(1-cyclopropylethoxy)-2,5-dimethyl-4-nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309191B2
Source datasetuspto-grants-2016_04
ORD IDord-81d80c4b3eb749bbb8ca63be0e8bf261
Source noteuspto-grants-2016_04