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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295191Generated: October 30, 2026

cis-1-Ethoxy-2-(tri-n-butylstannyl)ethylene → HCID 21471346, compound

https://huagongshe.com/reaction/2295191

Reaction equation

Participants

RoleNameHCIDCharge
Reactantcis-1-Ethoxy-2-(tri-n-butylstannyl)ethyleneHCID 5706773—
ReactantHCID 21471359HCID 21471359—
ReactantHCID 86597747HCID 86597747—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21471346HCID 2147134676%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-BuLi (1.6M in hexanes, 1.52 ml, 2.43 mmol) was added to a solution of cis-1-ethoxy-2-(tri-n-butylstannyl) ethylene (1.06 gm, 2.94 mmol) in dry THF (7.5 ml) at -78° C. The mixture was stirred for 11/4 hours, then cooled to -100° C. (liquid N2 /methanol) and treated with a solution of 4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinecarboxaldehyde (707 mg, 2.43 mmol) in THF (3.0 ml). Forty-five minutes after the addition, the temperature was raised to -78° C. and the mixture was stirred for an additional 50 minutes. The solution was then stirred in an ice bath for 5 minutes and subsequently quenched with H2O (8 ml) and 10% HCl (8 ml). After stirring at room temperature for 1.5 hours, the mixture was made basic with 10% NaOH (10 ml) and extracted twice with Et2O. The combined Et2O layers were washed with H2O and brine, dried (Na2SO4), filtered and stripped to yield a solid. The solid was washed with cold Et2O. The Et2O washings were stripped and triturated with cold hexane to give additional solid, which was pooled with the above solid to give 586 mg (76%) (E)-3-[4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinyl]-2-propenal. Analytically pure material was obtained by recrystallization from hot hexane/EtOAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691322
Source datasetuspto-grants-1997_11
ORD IDord-adbed90ac63741fea38a7f44477cbaf2
Source noteuspto-grants-1997_11