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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480155Generated: October 30, 2026

Methyltriphenylphosphonium chloride → HCID 178435233, compound

https://huagongshe.com/reaction/480155

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 aqeuous NH4Cl (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 numberUS06649600B1
Source datasetuspto-grants-2003_11
ORD IDord-59076620d7f542dbacc2cc7abd315a84
Source noteuspto-grants-2003_11