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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457729Generated: October 30, 2026

Diethyl Ether → ethyl 5-{(2RS,3RS)-3-amino-2-(4-nitrophenyl)butyl}-2-furancarboxylate

https://huagongshe.com/reaction/1457729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl 5-{(2RS,3RS)-3-azido-2-(4-nitrophenyl)butyl}-2-furancarboxylateHCID 54125754—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productethyl 5-{(2RS,3RS)-3-amino-2-(4-nitrophenyl)butyl}-2-furancarboxylateHCID 5373455696.2%

Reaction Steps

3.24 g of ethyl 5-{(2RS,3RS)-3-azido-2-(4-nitrophenyl)butyl}-2-furancarboxylate was dissolved in a mixed solution of 50 ml of tetrahydrofuran and 5 ml of water, and 2.37 g of triphenylphosphine was added thereto, followed by heating and refluxing for 6 hours. The reaction solution was left to cool to room temperature, and then ethyl ether and water were added thereto for extraction. The organic layer was washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The drying agent was filtered off, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1→20/1) to obtain 2.89 g of the above-identified compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849747
Source datasetuspto-grants-1998_12
ORD IDord-8c004830b49747909b3b1a417565a5bd
Source noteuspto-grants-1998_12