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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105680Generated: October 31, 2026

Methyltriphenylphosphonium chloride → HCID 178435233, compound

https://huagongshe.com/reaction/2105680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyltriphenylphosphonium chlorideHCID 9879809—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178456486HCID 178456486—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178435233HCID 17843523338%

Reaction Steps

To a stirred suspension of methyl triphenylphosphonium chloride (1.07 g, 3.0 mmol) in THF (20 ml) at 0° C. was added n-BuLi (1.4 M in hexane, 2.14 ml, 3.0 mmol). The resulting reddish-brown mixture was stirred at this temperature for 0.5 h and then at rt for 0.5 h. A solution of 4-(2,6-dioxo-1,3-dipropyl-2,3,6,9-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]octane-1-carbaldehyde (372 mg, 1.0 mmol) in THF (10 ml) was added over a period of 20 minutes and the resulting mixture was stirred overnight (12 h). The reaction mixture was partitioned between saturated aqueous NH2Cl2 (20 ml) and EtOAc (20 ml) and the aqueous phase was extracted with EtOAc (20 ml). The combined organic extracts were washed with saturated aqeuous NaCl (50 ml), dried (MgSO4), filtered and evaporated in vacuo to afford an oil that was purified by radial chromatography (2 mm plate) using a gradient of 0-5% MeOH in CH2Cl2 as eluent. Product-containing fractions were combined and concentrated to afford 140 mg (38%) of a white solid. MS: 371 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579354B2
Source datasetuspto-grants-2009_08
ORD IDord-2e1c59752f48484b9d2eb90a785e6de1
Source noteuspto-grants-2009_08