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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581040Generated: October 31, 2026

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

https://huagongshe.com/reaction/581040

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 numberUS05919786
Source datasetuspto-grants-1999_07
ORD IDord-9f33cc1b1a0d4ef5b4402c31df59d396
Source noteuspto-grants-1999_07