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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30825Generated: October 25, 2026

Triethylborane → 2-(2-Fluoro-5-nitrophenyl)-2-methylpent-4-enal

https://huagongshe.com/reaction/30825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylboraneHCID 7357—
ReactantAllyl AlcoholHCID 7858—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantLithium ChlorideHCID 433294—
Reactant2-(2-Fluoro-5-nitrophenyl)propanalHCID 86600438—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product2-(2-Fluoro-5-nitrophenyl)-2-methylpent-4-enalHCID 86600439—

Reaction Steps

To a solution of palladium acetate (0.1 eq), triphenylphosphine (0.2 eq), lithium chloride (1.0 eq) in THF were sequentially added 2-(2-fluoro-5-nitrophenyl) propanal (1.1 eq) in THF, allyl alcohol (1.0 eq), triethylamine (1.2 eq) and triethylborane (2.4 eq) under nitrogen at room temperature. Solution was allowed to stir for 2 h. Mixture was diluted with saturated solution of sodium bicarbonate, extracted with ethyl acetate. Organics were washed with brine, dried with sodium sulfate and concentrated. Crude product was purified using flash chromatography (85% Hex: 15% EtoAc) on silica to afford 2-(2-fluoro-5-nitrophenyl)-2-methylpent-4-enal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423150B2
Source datasetuspto-grants-2008_09
ORD IDord-c0ef632ba96748608141c61764770d25
Source noteuspto-grants-2008_09