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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430478Generated: October 30, 2026

Hexane → HCID 70014587, compound

https://huagongshe.com/reaction/430478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-(m-nitrophenyl)-3-oxopropionateHCID 104078—
Reactant2-Butene, 1-bromo-HCID 122414—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70014587HCID 7001458775%

Reaction Steps

A 60% dispersion of NaH in mineral oil (917 mg, 22.9 mmol) was added over 20 min to a solution of ethyl 3-nitro-β-oxobenzenepropanoate (5.00 g, 21.1 mmol) in THF (50 mL) at such a rate to maintain a gentle reflux. The mixture was stirred at 25° for 30 min and a solution of crotyl bromide (2.95 g, 21.9 mmol) in THF (15 mL) was added over 50 min. The reaction mixture was stirred at 25° for 45 min and then heated at reflux for 16 h. Hexane (100 mL) was added to the cooled mixture. The resulting suspension was filtered and the filtrate was concentrated under reduced pressure. The residue was dissolved in EtOAc and the resulting solution was washed with aqueous 10% citric acid (2×), aqueous saturated NaHCO3 (2×) and brine then was dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash chromatography (40-63μ silica gel, hexane:EtOAc, 9:1) to afford ethyl α-(2-butenyl)-3-nitro-β-oxobenzenepropanoate (4.60 g, 75% yield):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323202B1
Source datasetuspto-grants-2001_11
ORD IDord-9daf679ff96d4331a151bc6477df223f
Source noteuspto-grants-2001_11