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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626315Generated: November 1, 2026

Triphenylphosphine → HCID 117620618, compound

https://huagongshe.com/reaction/626315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(2-Methylcyclopropyl)methanolHCID 138655—
Reactant2,5-Dimethyl-4-nitrophenolHCID 282110—
ReactantSodium BicarbonateHCID 516892—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
SolventTolueneHCID 1140—
ProductHCID 117620618HCID 11762061883.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

2.55 g of Bis(2-methoxyethyl) azodicarboxylate was added to a mixture of 1.40 g of 2,5-dimethyl-4-nitrophenol, 0.72 g of (2-methylcyclopropyl)methanol, 2.64 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 1.64 g of 2,5-dimethyl-1-[(2-methylcyclopropyl)methoxy]-4-nitrobenzen e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309191B2
Source datasetuspto-grants-2016_04
ORD IDord-4c97c1f8c43246b99592aad71af0e8b7
Source noteuspto-grants-2016_04